Home

WAGR syndrome

Síndrome WAGR - Wikipedia, la enciclopedia libr

WAGR syndrome - Wikipedi

  1. It occurs in about half of individuals with WAGR syndrome. The tumor usually develops between the ages of 1 and 3 years. Most cases are detected by age 8, but in rare cases it has occurred later. Babies with WAGR syndrome should have ultrasounds of their abdomen at birth and then every 3 months until age 8 years
  2. Correlación genotipo-fenotipo El Síndrome WAGR es un clásico síndrome de genes contiguos causado por una deleción de tamaño variable en el brazo corto del cromosoma 11. La región incluye más de 100 genes, algunos de ellos de función desconocida
  3. The International WAGR Syndrome Association is a not-for-profit organization comprised of an international network of families, health care professionals and researchers, and others who care for individuals with WAGR syndrome

The WORLD AMATEUR GOLF RANKING® ranks male and female amateur golfers by assessing performance at thousands of amateur golf tournaments and championships, worldwide In people with WAGR syndrome, Aniridia occurs as a result of a deletion of one copy of the gene called PAX6. This gene is located on the short (p) arm of Chromosome 11. This type of Aniridia is usually not inherited. Learn More - Genetics of WAGR Syndrome It is a collection of standardized information about individuals diagnosed with WAGR syndrome, Aniridia, and/or 11p deletions. The Registry is designed to collect and organize data that will help researchers to better characterize and understand the numerous conditions associated with WAGR syndrome, and to potentially develop effective treatments and therapies WAGR syndrome stands for Wilms' tumor, aniridia, genitourinary anomalies, and mental retardation, which is now called intellectual disability, and this is a genetic disorder that's caused when a part of chromosome 11 is missing, or deleted

Abstract. Objective: WAGR syndrome is a rare syndrome which involves microdeletions of the short arm of chromosome 11 at band 11p13. The clinical features are Wilms' tumor, aniridia, genitourinary abnormalities and mental retardation. There are very few reported cases. We report a new case of WAGR syndrome and review the literature WAGR syndrome. WAGR syndrome also called 11p deletion syndrome, is a rare genetic syndrome that affects many body systems and is named for its main features: Wilms tumor, Anirida, Genitourinary anomalies such as undescended testicles or hypospadias in males, or internal genital or urinary anomalies in females, and Range of developmental delays such as intellectual disability (mental.

Síndrome WAGR Genetic and Rare Diseases Information

  1. WAGR Syndrome in Children What is WAGR syndrome? WAGR syndrome, or WAGR complex, is a genetic disorder that affects the kidneys, urinary tract, genitalia, eyes and mental abilities. The acronym WAGR stands for Wilms tumor, aniridia, genitourinary malformations and a range of mental disabilities
  2. It is also an occasion to learn about current research and new therapies and treatments for WAGR syndrome, as well as updates on the activities of the International WAGR Syndrome Association. Each year, WAGR Weekend takes place in a different location, and is hosted by an IWSA family
  3. The WAGR syndrome or complex stands for: Wilms tumors (greatly increased risk
  4. WAGR syndrome is a rare genetic disorder characterized by a de novo deletion of 11p13 and is clinically associated with Wilms' tumor, aniridia, genitourinary anomalies, and mental retardation (W-A-G-R). Although the genotypic defects in WAGR syndrome have been well established, the large variety of phenotypic manifestations of the syndrome has never been reported
  5. Síndrome WAGR síntomas, causas, medicamentos, diagnóstico, y diagnósticos erróneos. El incluir otro diagnosis y verificador de síntomas
  6. WAGR syndrom, delesjon, Wilms tumor 1 (WT1) genet WAGR syndrom er forkortelse for Wilms tumor-Aniridi-Genitale avvik-Retardasjon av vekst og utvikling syndrom. En god del av den medisinske litteraturen som beskriver WAGR syndrom er skrevet før man forsto hvor forskjellig syndromet kan arte seg fra person til person. I dag vet man for eksempel at flertallet, Fortsett å lese «WAGR.

WAGR syndrome Genetic and Rare Diseases Information

  1. A group of symptoms that collectively indicate or characterize a disease, disorder, or other condition considered abnormal. 2
  2. gly disparate areas of the body, including the kidney, the GU system, the iris of the eye, and the CNS. The deletion of varying lengths of chromosomal material along the short arm of chromosome 11 is the underlying defect, and developmental abnormalities are related to the contiguous loss of neighboring genes
  3. WAGR syndrome is a rare genetic syndrome in which there is a predisposition to several conditions, including certain malignancies, distinctive eye abnormalities, and/or intellectual disability. WAGR is an acronym for Wilms tumor, Aniridia, Genitourinary problems (such as undescended testicles or hypospadias in males, or internal genital or urinary anomalies in females), and Range of.

About WAGR Syndrome - Genome

The patient was born with aniridia and cryptorchidism. At the age of 4 years, he was diagnosed with WAGR (Wilms' tumor, aniridia, genitourinary anomalies, and a range of developmental delays) syndrome, which was confirmed by fluorescence in situ hybridization, revealing deletion of the WT1 and PAX6 genes on chromosome 11p13 El Síndrome WAGR, también llamado Síndrome del tumor Wilms-aniridia o es una enfermedad rara genética cuyos afectados están predispuestos a desarrollar el llamado tumor de Wilms (un tumor que afecta a los riñones), junto con Aniridia (ausencia del iris del ojo), trastornos Genitourinarios, y Retraso mental. [1] La G es interpretada a veces como gonadoblastoma, ya que los trastornos. WAGR syndrome/11p deletion syndrome is a rare genetic syndrome in which there is a predisposition to several conditions, including certain malignancies, distinctive eye abnormalities, and/or intellectual disability. WAGR is an acronym for the characteristic abnormalities associated with the syndrome

About WAGR - What is WAGR Syndrome

  1. WAGR (Wilms' tumor, aniridia, genitourinary anomalies, and a range of developmental delays) syndrome, which was confirmed by fluorescence in situ hybridization, revealing deletion of the WT1 and PAX6 genes on chromosome 11p13
  2. WAGR syndrome (also known as WAGR complex, Wilms tumour-aniridia syndrome, aniridia-Wilms tumour syndrome) is a rare genetic syndrome in which affected children are predisposed to develop Wilms tumour (a tumour of the kidneys), Aniridia (absence of the coloured part of the eye, the iris), Genitourinary anomalies, and mental Retardation
  3. El síndrome WAGR es una rara alteración genética caracterizada por una deleción de novode 11p13, y se asocia clínicamente con el tumor de Wilms, la ani- ridia, las anomalías genitourinarias y el retraso inte
  4. El síndrome de WAGR es debido a una deleción de material genético en el brazo corto del cromosoma 11. El tamaño de la deleción varía entre los individuos afectados. Los signos y síntomas del síndrome de WAGR están relacionados con la pérdida de múltiples genes en el brazo corto del cromosoma 11
  5. The Men's Ranking within the WORLD AMATEUR GOLF RANKING® system ranks amateur golfers on the basis of their average performance in Counting Events over a rolling cycle of the last 104 weeks

WAGR syndrome is a rare genetic disorder characterized by a de novo deletion of 11p13 and is clinically associated with Wilms' tumor, aniridia, genitourinary anomalies, and mental retardation.. WAGR syndrome Disease definition A rare genetic disorder characterized by an unusual complex of congenital developmental abnormalities with intellectual disability, and an increased risk of developing Wilms tumor WAGR syndrome consists of Wilms tumor, aniridia, genitourinary anomalies, and mental retardation, and is caused by deletions of 11p13 and hemizygosity in this region. Further, the phenotype caused by the deletions suggested that there was a tumor suppressor in this region related to Wilms tumor (for a review, see Hastie 67). In Denys-Drash syndrome, there is a complex nephropathy and sexual ambiguity WAGR syndrome is a genetic syndrome in which there is a predisposition to several conditions, including certain malignancies, distinctive eye abnormalities, and/or mental retardation. WAGR is an acronym for Wilms tumor, Aniridia, Genitourinary anomalies (such as undescended testicles or hypospadias in males, or internal genital or urinary anomalies in females), mental Retardation syndrome When WAGR syndrome includes obesity starting in childhood, it is often called WAGRO syndrome. WAGR syndrome is due to a deletion of genetic material on the short arm of chromosome 11. The deletion size varies between individuals affected. Signs and symptoms of WAGR syndrome are related to the loss of multiple genes on the short arm of.

Estadísticas de Síndrome WAGR 0 personas con Síndrome WAGR han realizado el cuestionario SF36. La media de Síndrome WAGR es 0 puntos (0 %). La puntuación oscila entre 0 y 3.600, siendo 0 la peor y 3.600 la mejor Range of developmental delays. People with Wagr Syndrome can experience a range (the R of Wagr Syndrome) of developmental delays. Learning difficulties, psychiatric problems like anxiety, depression, and others, and behavioral problems like OCD (obsessive compulsive disorder) and ADHD (attention deficit hyperactivity disorder) are not uncommon in Wagr Syndrome

International WAGR Syndrome Associatio

Urology: After aniridia, GU abnormalities, and mental retardation (AGR) syndrome or Wilms tumor aniridia, GU abnormalities, and mental retardation (WAGR) syndrome is diagnosed, GU abnormalities.. WAGR syndrome: is the 'R' always justified? Termine C(1), Parigi G, Rossi M, Romano P, Balottin U. Author information: (1)Child Neuropsychiatry Unit, Department of Clinical and Biological Sciences, University of Insubria and Ospedale Fondazione Macchi, Varese, Italy. cristiano.termine@uninsubria.i

WAGR syndrome is characterized by Wilms' tumor (W), aniridia (A), genitourinary anomalies (G) and mental retardation (R). In the early human fetus, WT-1 is expressed in the pleural and abdominal mesothelium, and consequently this gene may play a role in diaphragm development Overview. WAGR syndrome is a disorder that affects many body systems and is named for its main features: Wilms tumor, anirida, genitourinary anomalies (such as undescended testicles or hypospadias in males, or internal genital or urinary anomalies in females), and intellectual disability (formerly referred to as mental retardation) WAGR is a rare syndrome with high mortality in children. Pancreatitis is a well-recognised and life-threatening association with the WAGR syndrome. However, there are no treatment guidelines to prevent relapsing, recurrent pancreatitis in WAGR syndrome

The World Amateur Golf Rankings® (WAGR®) The Official

Finally Ella's blood was analysed at the Centre for Life and she was diagnosed with WAGR syndrome, a rare chromosome disorder. Family can finally begin to enjoy life; WHEN James and Elly Chapple's first child Ella was diagnosed with a rare disorder that affects one in 800,000 babies, their lives were turned upside down WAGR syndrome is a rare genetic condition that can affect both boys and girls. Babies born with WAGR syndrome often have eye problems, and are at high risk for developing certain types of cancer, and a range of developmental delays WAGR syndrome (also known as WAGR complex, Wilms tumour-aniridia syndrome, aniridia-Wilms tumour syndrome) is a rare genetic syndrome in which affected children are predisposed to develop Wilms tumour (a tumour of the kidneys), Aniridia (absence of the coloured part of the eye, the iris), Genitourinary anomalies, and mental Problems. [1] The G is sometimes instead given as gonadoblastoma. WAGR syndrome is associated with contiguous gene deletions involving both PAX6 and the adjacent WT1 gene on chromosome 11p13. The PAX6 gene encodes highly conserved transcriptional factors that are involved in the early development of the eye, brain, olfactory bulb, neural tube, pancreas and gut in the embryo

Aniridia may also be one of the features associated with the WAGR syndrome. Aniridia Europe cooperates with the International WAGR Syndrome Association (IWSA). Please visit wagr.org for further information. A full session about WAGR Syndrome was also included in the 3rd European Conference on Aniridia in 2016 WAGR Syndrome is an uncommon disease that can affect both genders. It is more common for babies to be born with the syndrome, rather than getting diagnosed with the disease later on in life. The babies that are born with WAGR face high risks of being diagnosed with cancer, can develop eye problems, as well as a delay with their mental progress Fischbach BV, Trout KL, Lewis J. WAGR syndrome: A clinical review of 54 cases. Pediatrics. Oct 2005. 116:984-988. Dahan K, Kamal M, Noel LH, et al. Small glomeruli in WAGR syndrome (Wilms tumor, aniridia, genitourinary anomalies and mental retardation) syndrome. Am J Kidney Dis. June 2007. 49:522-527

WAGR Syndrome Add Wilms Tumor, Aniridia, Genitourinary Anomalies, And Mental Retardation Syndrome Add Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation Syndrome Add Wilms Tumor-Aniridia-Genital Anomalies-Retardation Syndrome Add Wilms Tumor-Aniridia-Genitourinary Anomalies. DID YOU KNOW..... The IWSA offers a private, online support g... roup for parents and primary caregivers of individuals with WAGR Syndrome? It is a private, confidential place for parents of children/adults with WAGR Syndrome to share their triumphs and challenges WAGR syndrome (Wilms tumor, aniridia, genitourinary anomalies, and range of developmental delays) is a rare genetic condition with an increased risk of developing Wilms tumor. In this study, 43 patients with WAGR and Wilms tumor (or Wilms tumor precursor lesions/nephroblastomatosis) were identified International WAGR Syndrome Association (IWSA), Montgomery Village, Maryland. 1,337 likes · 4 talking about this · 12 were here. With more than 250 members in 42 countries around the world, there is.. International WAGR Syndrome Association (IWSA), Montgomery Village, Maryland. 1,336 likes · 18 talking about this · 12 were here. With more than 250 members in 42 countries around the world, there is..

About WAGR - A is for Aniridi

The WAGR syndrome is a multiple congenital anomaly-mental retardation syndrome caused by interstitial deletion of the distal portion of chromosome 11p13 International WAGR Syndrome Association (IWSA), Montgomery Village. 1.336 Me gusta · 13 personas están hablando de esto · 12 personas estuvieron aquí. With more than 250 members in 42 countries.. Animated Mnemonics (Picmonic): https://www.picmonic.com/viphookup/medicosis/ - With Picmonic, get your life back by studying less and remembering more. Med..

Research - WAGR Syndrome Patient Registr

  1. Statistics of WAGR Syndrome - 11p Deletion Syndrome Map - Check how this condition affects the daily life of people who suffer it
  2. Aniridia and WAGR Syndrome: A Guide for Patients and Their Families Author: Jill Ann Nerby published on April, 2010: Amazon.es: Libro
  3. World map of WAGR Syndrome - 11p Deletion Syndrome Find people with WAGR Syndrome - 11p Deletion Syndrome through the map. Connect with them and share experiences. Join the WAGR Syndrome - 11p Deletion Syndrome community
  4. Living with WAGR Syndrome - 11p Deletion Syndrome can be difficult, but you have to fight to try to be happy. Have a look at things that other people have done to be happy with WAGR Syndrome - 11p Deletion Syndrome. World map of WAGR Syndrome - 11p Deletion Syndrome View more. Toggle navigation. WAGR Syndrome - 11p Deletion Syndrome
  5. WAGR Syndrome Patient Registry Campaign 2020. In August 2020, the IWSA hosted a campaign to increase participation in the WAGR Syndrome Patient Registry. We created a series of videos with parents, physicians, researchers, and children/
  6. International WAGR Syndrome Association (IWSA), Montgomery Village, Maryland. 1,296 likes · 3 talking about this · 13 were here. With more than 250 members in 38 countries around the world, there is..
  7. Aniridia y Síndrome de WAGR. Reporte de 6 casos clínicos en el Hospital Civil de Culiacán Rafael Ortiz-Zavala, a* Ruth Acuña-Maldonado, a Cristina Villanueva-Mendoza, b Gilma López-López a a Departamento de Ginecología y Obstetricia. Centro de Investigación y Docencia en Ciencias de la Salud, Universidad Autónoma de Sinalo

Wilms tumor, aniridia, genitourinary anomalies, and mental retardation (WAGR) syndrome is a contiguous gene deletion syndrome involving the Wilms tumor 1 gene (WT1), the paired box gene 6 (PAX6), and possibly other genes on chromosome 11p13. WT1 is required for normal formation of the genitourinary The following tests and methods are typically employed for the diagnosis of WAGR Syndrome: A thorough physical examination An evaluation of family history (although in most cases, a family medical history may not be very helpful) An assessment of symptoms: The earliest manifested symptom is. WAGR syndrome is caused by a deletion on chromosome 11 inclusive of both WT1 and the PAX6 gene, which is associated with aniridia. Aniridia is characterized by bilateral underdevelopment or absence of iris tissue and is typically the first noticeable sign of WAGR syndrome Background: Wilms tumor, aniridia, genitourinary anomalies and mental retardation (WAGR) syndrome is a rare genetic disorder caused by heterozygous deletions of WT1 and PAX6 at chromosome 11p13. Deletion of BDNF is known eto be associated with hyperphagia and obesity in both humans and animal models; however, neuroendocrine and epigenetic profiles of individuals with WAGR syndrome remain to be determined

WAGR syndrome - Osmosi

WAGR syndrome is called a contiguous gene deletion syndrome. This means that it is caused by the loss of a section of genes on chromosome 11 (11p13). Most of the time the changes on chromosome 11p13 happen by chance when the egg or sperm are being formed or during the very early stages of the baby's development in the womb 18. Ivanov I, Shuper A, Shohad M, Snir M, Weitz R. Aniridia, PAX6 gene, WAGR syndrome and the risk of neoplastic proliferation. Cancer Detect Prev. 1996;20. 19. Chao L, Huff V, Strong LC, Saunders GF. Mutation in the PAX6 gene in twenty patients with aniridia. Hum Mutat. 2000;15:332-9. 20. Amor DJ. Morbid obesity and hyperphagia in the WAGR. 1. Nihon Rinsho. 2006 Sep 28;Suppl 3:605-8. [WAGR syndrome]. [Article in Japanese] Kaneko Y(1). Author information: (1)Research Institute for Clinical Oncology, Saitama Cancer Center. PMID: 17022619 [Indexed for MEDLINE WAGR 11p13 deletion syndrome is associated with abnormalities including (W) ilms tumor, (A) niridia, (G) enitourinary abnormalities, and growth and mental (R) etardation (WAGR). Potocki-Schaffer syndrome is a contiguous gene syndrome associated with deletions in 11p11.2, principal features of which are multiple exostoses, parietal foramina development delay, mental retardation, and facial dysmorphism Browse latest WAGR® Counting Events Men's Events. While we endeavour to ensure that the information on the Website is correct, event information, dates and venues are provided to us by the event organisers. We do not warrant and will not be liable for the accuracy and completeness of such information

Aniridia, Wilms tumor, genitourinary abnormalities, growth and mental retardation are the cardinal features of the WAGR 11p13 deletion syndrome. The Potocki-Schaffer syndrome or proximal 11p deletion syndrome (previously DEFECT11 syndrome) is a contiguous gene syndrome associated with deletions in 1 WAGR syndrome's a genetic disorder that can involve several symptoms, including Wilms' tumor, aniridia, genitourinary abnormalities, a... What is WAGR syndrome From GHR WAGR syndrome is a disorder that affects many body systems and is named for its main features: Wilms tumor, aniridia, genitourinary anomalies, and intellectual disability (formerly referred to as mental retardation).People with WAGR syndrome have a 45 to 60 percent chance of developing Wilms tumor, a rare form of kidney cancer

WAGR syndrome, the risk has been estimated to up to 45%. The median age at diagnosis is earlier than average age (17-27 months versus 38 months)12 Ther The International WAGR Syndrome Association promotes awareness, stimulates research, and supports families affected by WAGR syndrome. The syndrome is ultra rare, with less than 500 diagnosed cases worldwide, and the IWSA provides information for families, physicians, researchers, educators and others in an effort to improve the quality of life for individuals with WAGR syndrome AGR syndrome is a subgroup of WAGR syndrome in which patients do not develop Wilms tumor and is associated with deletion of chromosome 11p14.1-p13, where the LGR4 gene (GPR48; 606666) is located. Yi et al. (2014) found that mice lacking Lgr4 had aniridia, polycystic kidney disease, genitourinary abnormalities, and mental retardation, similar to the pathologic defects of AGR syndrome

WAGR Syndrome and the WT1 Gene There is a high risk of Wilms Tumours in isolated cases of aniridia, particularly when the patient also has genitourinary abnormalities and learning disability (mental retardation), the so-called Wilms Tumours-aniridia-genital abnormality-mental retardation (WAGR) syndrome WAGR syndrome. An AD complex characterized by Wilms' tumor-WT, aniridia, genitourinary abnormalities-renal agenesis, gonadoblastoma, mental retardation. McGraw-Hill Concise Dictionary of Modern Medicine. © 2002 by The McGraw-Hill Companies, Inc

WAGR syndrome causes, symptoms, diagnosis, treatment

El síndrome Beckwith-Wiedemann (SBW) es una enfermedad genética o epigenética de sobrecrecimiento asociada con un elevado riesgo de formación de tumor embriónico. [1] La enfermedad es causada por mutaciones en genes reguladores del crecimiento en el cromosoma 11(en la región 11p15.5) o por errores en impronta genómica. [2] Los pacientes presentan de forma típica vísceras fuera de la. International WAGR Syndrome Association (IWSA), Montgomery Village, Maryland. 1,237 likes · 16 talking about this · 5 were here. With more than 250 members in 38 countries around the world, there is.. WAGR may refer to: . WAGR (AM), a radio station (1340 AM) licensed to Lumberton, North Carolina, United States WAGR-FM, a radio station (102.5 FM) licensed to Lexington, Mississippi, United States; WAGR syndrome; Western Australian Government Railways; Wilms tumor 1, a protein; The Windscale Advanced gas-cooled reactor at Sellafield; World Amateur Golf Ranking, the R&A's global ranking system. The WAGR syndrome or complex stands for: Wilms tumors (greatly increased risk) aniridia genitourinary anomalies intellectual retardation (disability) Pathology Genetics Occurs from a mutation related to chromosome 11p13 3 which is in close..

Video: WAGR Syndrome in Children Children's Hospital Colorad

Individuals are at high risk (>30%) of having a Wilms tumor. At birth, the association is aniridia, GU malformations, and mental retardation (AGR) syndrome. With the discovery of a Wilms tumor in these patients, the association is referred to as WAGR syndrome Obesity and WAGR syndrome. February 2000; Clinical Dysmorphology 9(1):63-4; DOI: 10.1097/00019605-200009010-00014.

What is aniridia

Infobox_Disease Name = PAGENAME Caption = DiseasesDB = 14025 ICD10 = ICD9 = ICDO = OMIM = 194072 MedlinePlus = eMedicineSubj = ped eMedicineTopic = 242 WAGR syndrome is a rare genetic condition that affects multiple body systems. There are fewer than 500 known cases of this disorder. WAGR is an acronym that stands for Wilms tumor, Aniridia, Genitourinary abnormalities, and Range of developmental delays. A wide variety of other conditions are also associated with the syndrome. While some of these conditions are bein

Newly Diagnosed – WAGRAniridia - Causes, Symptoms, Diagnosis & TreatmentFlashcards - 5Genetic Syndrome Pictures - StudyBlueIntellectual Disability; Disability, Intellectual; Idiocy

WAGR complex, Wilms tumour-aniridia syndrome, aniridia-Wilms tumour syndrome. Clinical features and diagnosis. Newborn children with WAGR syndrome are soon noted to have aniridia. The clinical suspicion for WAGR may be increased with the presence of other genital anomalies, though genitourinary anomalies are not always present, particularly in. Definition of WAGR SYNDROME in the Definitions.net dictionary. Meaning of WAGR SYNDROME. What does WAGR SYNDROME mean? Information and translations of WAGR SYNDROME in the most comprehensive dictionary definitions resource on the web Find all the evidence you need on WAGR syndrome via the Trip Database. Helping you find trustworthy answers on WAGR syndrome | Latest evidence made eas The WAGR syndrome stands for: Wilms tumours (greatly increased risk) aniridia genital anomalies intellectual retardation (disability) Pathology Genetics Occurs from a mutation related to chromosome 11p13 3 which is in close proximity to th..

  • Walnuts benefits.
  • Nicko McBrain joven.
  • Porque se daña la cremallera de un auto.
  • Vestido de novia chino tradicional.
  • El castillo de cristal Sinopsis.
  • La cara oculta de la luna novela reparto.
  • Ford Ranger 2017 usada.
  • Mockup camisa polo gratis.
  • Que son las larvas.
  • Ragdoll precio Perú.
  • Fusilamiento de Che Guevara.
  • Cisternas usadas en venta.
  • Que pasa si cae un meteorito en el mar.
  • Productos de jardinería.
  • Ecocaribe teléfono.
  • Empleo Asistente administrativo computrabajo.
  • Noah Baumbach biografía.
  • Los quistes en los ovarios se mueven como un bebé.
  • Procesador CPU precio.
  • Burbujas de colores fondo de pantalla.
  • Maestros de la ilusión reparto.
  • Fotos De hombres alemanes.
  • Freak show song.
  • Thanksgiving significado.
  • Chicago Bulls campeonatos.
  • Esto es guerra final 2018.
  • Películas de Donnie Yen mega.
  • Chicas en moto con casco.
  • Imagen de reclutamiento de personal.
  • Cabañas la Marina Ajusco.
  • Dharma vs karma.
  • Icono de Safari.
  • Imagenes de comida chistosa.
  • Tuición sinónimo.
  • Imágenes de Taza de café.
  • Portadas de Ciencias naturales para niños.
  • Rana dorada Panamá.
  • Locomotora eléctrica características.
  • Bernes de la Montaña Guadalajara.
  • Similitud de una cefalosporina con una penicilina.
  • Boiling point of water.