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¿qué es 'Síndrome de Apert - trastorno congénito que afecta primero arco branquial '?
Definición de Síndrome de Apert
Apert Syndrome, virtually synonymous with Acrocephalosyndactyly, is a branchial arch syndrome, resulting from a developmental anomaly.
más
Apert Syndrome, virtually synonymous with Acrocephalosyndactyly, is a branchial arch syndrome, resulting from a developmental anomaly. Specifically, this syndrome affects the first branchial (or pharyngeal) arch, which is the precursor of the maxilla and mandible. Since the branchial arches are important developmental features in a growing embryo, disturbances in its development create lasting and widespread effects.
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do i have 'Síndrome de Apert'?
Además las siguientes pruebas de diagnóstico puede ser necesario para ayudar a verificar el diagnóstico:
prueba de diagnóstico de los resultados de la búsqueda 'Síndrome de Apert'
1 - 5 of
16
pruebas de diagnóstico
Los estudios de genética molecular
Síndrome de Apert y Los estudios de genética molecular
Audiencia de prueba
standard technique of representing hearing loss
Síndrome de Apert y Audiencia de prueba
Pruebas psicométricas
Síndrome de Apert y Pruebas psicométricas
X-ray foot (feet)
Síndrome de Apert y X-ray foot (feet)
X-ray hand(s)
Síndrome de Apert y X-ray hand(s)
De rayos X del cráneo
Síndrome de Apert y De rayos X del cráneo
De rayos X columna vertebral
Síndrome de Apert y De rayos X columna vertebral
X-rays
Síndrome de Apert y X-rays
RM cerebral
Síndrome de Apert y RM cerebral
CT cerebro
Síndrome de Apert y CT cerebro
CT scan
Síndrome de Apert y CT scan
Developmental testing
Síndrome de Apert y Developmental testing
Neuropsychiatric evaluation
Síndrome de Apert y Neuropsychiatric evaluation
Psychologic Evaluation and support
Síndrome de Apert y Psychologic Evaluation and support
discurso de recepción umbral de la TER
Síndrome de Apert y discurso de recepción umbral de la TER
ultrasound 3D cranial sutures
Síndrome de Apert y ultrasound 3D cranial sutures
para obtener más ingreso por favor, es de acceso libre (haga clic aquí para acceder)
procedimientos terapéuticos para 'Síndrome de Apert'?
La gestión o tratamiento de enfermedades debe ser siempre determinada por un proveedor de servicios de salud los pacientes. Abajo hay una lista de asociados procedimientos terapéuticos o medicamentos para Apert's Syndrome:
procedimiento terapéutico de los resultados de la búsqueda 'Síndrome de Apert'
1 - 5 of
5
procedimientos terapéuticos
rankings are computer generated. por favor consulte a su proveedor de servicios de salud.
Reconstrucción craneofacial
Síndrome de Apert y Reconstrucción craneofacial
Educación Especial
Síndrome de Apert y Educación Especial
Terapia del habla
Síndrome de Apert y Terapia del habla
X-ray foot (feet)
Síndrome de Apert y X-ray foot (feet)
remodelación quirúrgica del cráneo
Síndrome de Apert y remodelación quirúrgica del cráneo
medicamentos para los resultados de la búsqueda 'Síndrome de Apert'
rankings are computer generated. por favor consulte a su proveedor de servicios de salud.
resultados de la búsqueda web para 'Síndrome de Apert'?
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Resultados
1 - 50
- Síndrome de Apert
[Apert's syndrome (acrocephalosyndactylia]
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1: Orv Hetil. 1974 Sep 8;115(36):2127-30. [Apert's syndrome (acrocephalosyndactylia] [Article in Hungarian] Ruppert F, Schultz K, Weisenbach J, Bozzay L. Mesh Terms: ...
http://www.ncbi.nlm.nih.gov/pubmed/4605511
www.ncbi.nlm.nih.gov
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summary
[Total facial osteotomy. Crouzon's syndrome, Apert's syndrome ...
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1: Ann Chir Plast. 1967 Dec;12(4):273-86. [Total facial osteotomy. Crouzon's syndrome, Apert's syndrome: oxycephaly, scaphocephaly, turricephaly] [Article in French] ...
http://www.ncbi.nlm.nih.gov/pubmed/5622570
www.ncbi.nlm.nih.gov
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Apert syndrome
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Apert syndrome is a genetic disease. It can be inherited or it may occur without ... family history of Apert syndrome. skeletal (limb) abnormalities ...
http://adam.about.com/encyclopedia/001581sym.htm
adam.about.com
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Apert syndrome - Wikipedia, the free encyclopedia
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Clinical assessment and multispecialty management of Apert syndrome" ... Apert Syndrome information from Seattle Children's Hospital Craniofacial Center ...
http://en.wikipedia.org/wiki/Apert_syndrome
en.wikipedia.org
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Apert syndrome - Genetics Home Reference
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Apert syndrome is a genetic disorder characterized by the ... abilities in people with Apert syndrome range from normal to ... Apert syndrome ...
http://ghr.nlm.nih.gov/condition=apertsyndrome
ghr.nlm.nih.gov
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summary
Apert Syndrome - Yahoo! Health
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Important It is possible that the main title of the report Apert Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name ...
http://health.yahoo.com/other-other/apert-syndrome/healthwise--nord254.html
health.yahoo.com
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summary
MedlinePlus Medical Encyclopedia: Apert syndrome
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Apert syndrome can be passed down through families (inherited) ... Apert syndrome is caused by mutations in a gene called fibroblast growth factor ...
http://www.nlm.nih.gov/medlineplus/ency/article/001581.htm
www.nlm.nih.gov
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summary
Apert syndrome
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Apert syndrome is a genetic disease in which the seams between the skull bones ... Apert syndrome can be passed down through families (inherited) ...
http://adam.about.com/encyclopedia/infectiousdiseases/Apert-syndrome.htm
adam.about.com
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summary
Carpenter syndrome - Wikipedia, the free encyclopedia
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Carpenter Syndrome belongs to a group of rare genetic disorders known as ... (Apert syndrome/Pfeiffer syndrome, Saethre-Chotzen syndrome, Carpenter syndrome, ...
http://en.wikipedia.org/wiki/Carpenter_syndrome
en.wikipedia.org
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101200
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http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=101200
www.ncbi.nlm.nih.gov
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Crouzon syndrome - Wikipedia, the free encyclopedia
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Specifically, this syndrome affects the first branchial (or pharyngeal) arch, ... Apert syndrome · Antley-Bixler syndrome · Pfeiffer syndrome · Crouzon syndrome ...
http://en.wikipedia.org/wiki/Crouzon_syndrome
en.wikipedia.org
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summary
Apert syndrome - References - Genetics Home Reference
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... Mohammadi M. Understanding the molecular basis of Apert syndrome. ... M. Apert syndrome. ... P, et al. Apert syndrome results from localized mutations of ...
http://ghr.nlm.nih.gov/condition=apertsyndrome/show/References
ghr.nlm.nih.gov
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summary
Apert syndrome and fetal hydrocephaly.
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Apert (1906) was the first to identify a syndrome characterized by the ... Since then Apert syndrome has been recognized as a clinical entity. ...
http://www.ncbi.nlm.nih.gov/pubmed/3519431
www.ncbi.nlm.nih.gov
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summary
Hearing loss with craniofacial syndromes - Wikipedia, the free encyclopedia
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Patients with Apert syndrome have a high occurrence of ... in Apert syndrome" ... For more information on Apert Syndrome. Overview of condition at NLM ...
http://en.wikipedia.org/wiki/Hearing_loss_with_craniofacial_syndromes
en.wikipedia.org
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A Biological Clock for Guys?
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A man's age may affect not only his ability to father a ... disorders such as autism and Apert's syndrome, as well as mental illnesses like schizophrenia. ...
http://www.webmd.com/parenting/features/guys-biological-clock
www.webmd.com
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summary
Holt-Oram syndrome - Wikipedia, the free encyclopedia
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Holt-Oram syndrome is caused by mutations in TBX5, a member of the ... (Apert syndrome/Pfeiffer syndrome, Saethre-Chotzen syndrome, Carpenter syndrome, ...
http://en.wikipedia.org/wiki/Holt-Oram_syndrome
en.wikipedia.org
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summary
Site Map od Pedbase.org - The Pediatric Database
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Pedbase Site Map. Pediatric. Site Map. Resources. Contact. PEDBASE.org - The Pediatric Database. A. B. C. D. E. F. G. H. I. J. K. L. M. N. O. P. R. S. T. U. V. W. X ...
http://pedbase.org/sitemap.html
pedbase.org
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MedlinePlus Medical Encyclopedia: Skeletal limb abnormalities
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... Marfan syndrome, Down syndrome, Apert syndrome, Basal cell nevus syndrome, and other conditions ... define a specific syndrome or condition or give a clue ...
http://www.nlm.nih.gov/medlineplus/ency/article/003170.htm
www.nlm.nih.gov
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summary
Möbius syndrome - Wikipedia, the free encyclopedia
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Möbius syndrome (also spelled Moebius) is an extremely rare congenital ... (Apert syndrome/Pfeiffer syndrome, Saethre-Chotzen syndrome, Carpenter syndrome, ...
http://en.wikipedia.org/wiki/M%C3%B6bius_syndrome
en.wikipedia.org
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Noonan syndrome - Wikipedia, the free encyclopedia
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Noonan Syndrome (NS) is a relatively common congenital genetic condition which ... (Apert syndrome/Pfeiffer syndrome, Saethre-Chotzen syndrome, Carpenter syndrome, ...
http://en.wikipedia.org/wiki/Noonan_syndrome
en.wikipedia.org
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Clinical assessment and multispecialty management of Apert syndrome.
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Clinical assessment and multispecialty management of Apert syndrome. Kaplan LC. ... issues that should be considered in all individuals with the Apert syndrome. ...
http://www.ncbi.nlm.nih.gov/pubmed/2065483
www.ncbi.nlm.nih.gov
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summary
Apert syndrome - Educational resources - Information pages - Genetics ...
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Ask the Geneticist: Inheritance of Apert syndrome. Children's Hospital Boston ... Orphanet: Apert syndrome. Orphanet: Craniosynostosis ...
http://ghr.nlm.nih.gov/condition=apertsyndrome/show/Educational+resources
ghr.nlm.nih.gov
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Encyclopedia A-Az on Yahoo! Health
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Health encyclopedia of diseases and conditions covering symptoms, definitions, ... Apert Syndrome. Aphasia. Aplasia Cutis Congenita. Apnea. Apnea, Infantile ...
http://health.yahoo.com/health/ency/
health.yahoo.com
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Pierre Robin syndrome - Wikipedia, the free encyclopedia
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... diaphragmatic hernia · Omphalocele · Gastroschisis · Prune belly syndrome ... (Apert syndrome/Pfeiffer syndrome, Saethre-Chotzen syndrome, Carpenter syndrome, ...
http://en.wikipedia.org/wiki/Pierre_Robin_syndrome
en.wikipedia.org
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Sakati-Nyhan-Tisdale syndrome - Wikipedia, the free encyclopedia
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A new syndrome with acrocephalopolysyndactyly, cardiac disease, and distinctive ... (Apert syndrome/Pfeiffer syndrome, Saethre-Chotzen syndrome, Carpenter syndrome, ...
http://en.wikipedia.org/wiki/Sakati-Nyhan-Tisdale_syndrome
en.wikipedia.org
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summary
Bones, muscles, and connective tissues - Genetics Home Reference
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Acrocephalosyndactyly (Apert) see Apert syndrome. acrocephalosyndactyly III see Saethre-Chotzen syndrome ... Apert syndrome. Appelt-Gerken-Lenz syndrome see ...
http://ghr.nlm.nih.gov/conditionCategory=bonesmusclesandconnectivetissues
ghr.nlm.nih.gov
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summary
Sotos syndrome - Wikipedia, the free encyclopedia
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Sotos syndrome (also known as cerebral gigantism) is a rare genetic disorder ... (Apert syndrome/Pfeiffer syndrome, Saethre-Chotzen syndrome, Carpenter syndrome, ...
http://en.wikipedia.org/wiki/Sotos_syndrome
en.wikipedia.org
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Congenital conductive hearing loss in Apert syndrome.
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... (Apert syndrome) is a rare craniosynostotic syndrome characterized ... We report three cases of conductive hearing loss in Apert syndrome. ...
http://www.ncbi.nlm.nih.gov/pubmed/3106904
www.ncbi.nlm.nih.gov
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summary
Zori Stalker Williams syndrome - Wikipedia, the free encyclopedia
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Zori Stalker Williams syndrome at NIH's Office of Rare Diseases ... (Apert syndrome/Pfeiffer syndrome, Saethre-Chotzen syndrome, Carpenter syndrome, ...
http://en.wikipedia.org/wiki/Zori_Stalker_Williams_syndrome
en.wikipedia.org
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CRANIOSYNOSTOSIS - Pedbase.org
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Apert Syndrome. Chotzen Syndrome. Pfeiffer Syndrome. Carpenter Syndrome. Crouzon Syndrome ... rule out syndrome. multidisciplinary Craniofacial Team. follow for ...
http://www.pedbase.org/c/craniosynostosis
www.pedbase.org
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Webbing of the fingers or toes
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Down syndrome. Hereditary syndactyly. Extremely rare causes: Apert syndrome. Carpenter syndrome. Cornelia de Lange syndrome. Pfeiffer syndrome. Smith-Lemli-Opitz ...
http://adam.about.com/encyclopedia/Webbing-of-the-fingers-or-toes.htm
adam.about.com
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summary
MedlinePlus Medical Encyclopedia:Craniofacial reconstruction - series ...
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birth defects (such as hypertelorism, Crouzon's disease, Apert's syndrome) ... Review provided by VeriMed Healthcare Network. ...
http://www.nlm.nih.gov/medlineplus/ency/presentations/100058_2.htm
www.nlm.nih.gov
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summary
Dubowitz syndrome - Wikipedia, the free encyclopedia
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Dubowitz syndrome is a rare genetic disorder characterized by microcephaly, ... (Apert syndrome/Pfeiffer syndrome, Saethre-Chotzen syndrome, Carpenter syndrome, ...
http://en.wikipedia.org/wiki/Dubowitz_syndrome
en.wikipedia.org
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A case of Pfeiffer syndrome.
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A case of Pfeiffer syndrome. Park MS, Yoo JE, Chung J, Yoon SH. ... Pfeiffer Syndrome is as rare as Apert syndrome in the Western population. ...
http://www.ncbi.nlm.nih.gov/pubmed/16614535
www.ncbi.nlm.nih.gov
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summary
Fountain syndrome - Wikipedia, the free encyclopedia
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Fountain syndrome is an autosomal recessive congenital disorder characterized by ... (Apert syndrome/Pfeiffer syndrome, Saethre-Chotzen syndrome, Carpenter syndrome, ...
http://en.wikipedia.org/wiki/Fountain_syndrome
en.wikipedia.org
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summary
Goldenhar syndrome - Wikipedia, the free encyclopedia
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Chief markers of Goldenhar syndrome are incomplete development of the ear, nose, ... (Apert syndrome/Pfeiffer syndrome, Saethre-Chotzen syndrome, Carpenter syndrome, ...
http://en.wikipedia.org/wiki/Goldenhar_syndrome
en.wikipedia.org
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summary
Keutel syndrome - Wikipedia, the free encyclopedia
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Keutel syndrome is a rare autosomal recessive genetic disorder characterized by ... (Apert syndrome/Pfeiffer syndrome, Saethre-Chotzen syndrome, Carpenter syndrome, ...
http://en.wikipedia.org/wiki/Keutel_syndrome
en.wikipedia.org
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APERT SYNDROME - Pedbase.org
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... for other malformations may be necessary - Type II (Apert-Crouzon Syndrome) ... 1994 -2007 Pedbase.org. Powered by Database of Pediatrics- APERT SYNDROME ...
http://pedbase.org/a/apert-syndrome/
pedbase.org
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Klippel-Trénaunay-Weber syndrome - Wikipedia, the free encyclopedia
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Klippel-Trénaunay-Weber Syndrome or KTS is a rare congenital medical condition ... (Apert syndrome/Pfeiffer syndrome, Saethre-Chotzen syndrome, Carpenter syndrome, ...
http://en.wikipedia.org/wiki/Klippel-Tr%C3%A9naunay-Weber_syndrome
en.wikipedia.org
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Nail-patella syndrome - Wikipedia, the free encyclopedia
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Nail-patella syndrome (NPS) is a genetic disorder that results in small, poorly ... (Apert syndrome/Pfeiffer syndrome, Saethre-Chotzen syndrome, Carpenter syndrome, ...
http://en.wikipedia.org/wiki/Nail-patella_syndrome
en.wikipedia.org
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Apert syndrome - MedlinePlus - Health information - Genetics Home Reference
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... information in the Genetics Home Reference condition summary on Apert syndrome. Encyclopedia: Apert syndrome. Encyclopedia: Webbing of the fingers or toes ...
http://ghr.nlm.nih.gov/condition=apertsyndrome/show/MedlinePlus
ghr.nlm.nih.gov
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summary
Overgrowth syndrome - Wikipedia, the free encyclopedia
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Overgrowth syndrome is a group of genetic disorders in which there is an ... (Apert syndrome/Pfeiffer syndrome, Saethre-Chotzen syndrome, Carpenter syndrome, ...
http://en.wikipedia.org/wiki/Overgrowth_syndrome
en.wikipedia.org
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Rubinstein-Taybi Syndrome -- GeneReviews -- NCBI Bookshelf
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... Pfeiffer syndrome and Apert syndromes), Saethre-Chotzen syndrome, and Greig ... part of the FGFR-related craniosynostosis syndromes are Pfeiffer syndrome, Apert ...
http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=rsts
www.ncbi.nlm.nih.gov
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Apert Syndrome - Yahoo! Health
[
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Apert Syndrome Pen Pals. National network. Founded 1992. Group correspondence program for persons with Apert syndrome to share experiences. ...
http://health.yahoo.com/children-nutrition/apert-syndrome/he...
health.yahoo.com
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Rubinstein-Taybi syndrome - Wikipedia, the free encyclopedia
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RTS - Rubinstein-Taybi Syndrome - A site devoted to the families and people ... (Apert syndrome/Pfeiffer syndrome, Saethre-Chotzen syndrome, Carpenter syndrome, ...
http://en.wikipedia.org/wiki/Rubinstein-Taybi_syndrome
en.wikipedia.org
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FGFR2 - fibroblast growth factor receptor 2 - Genetics Home Reference
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Apert syndrome - caused by mutations in the FGFR2 gene. Nearly all cases of Apert syndrome are caused by one of two mutations in the FGFR2 gene. ...
http://ghr.nlm.nih.gov/gene=fgfr2
ghr.nlm.nih.gov
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Yunis-Varon syndrome - Wikipedia, the free encyclopedia
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Yunis-Varon syndrome; Cleidocranial dysplasia, micrognathia, absent thumbs, ... (Apert syndrome/Pfeiffer syndrome, Saethre-Chotzen syndrome, Carpenter syndrome, ...
http://en.wikipedia.org/wiki/Yunis-Varon_syndrome
en.wikipedia.org
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The study of abnormal bone development in the Apert syndrome Fgfr2 ...
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Apert syndrome is caused by mutations in fibroblast growth factor receptor 2 ... The Apert syndrome Fgfr2+/S252W mouse model exhibits perinatal lethality. ...
http://www.ncbi.nlm.nih.gov/pubmed/18407821
www.ncbi.nlm.nih.gov
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9263565 1997 09 30 1997 09 30 2005 11 16 0735-1631 14 7 1997 Aug ...
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427-30 Apert Syndrome is characterized by craniosynostosis, bilateral syndactyly, ... A sixth case is reported here. Prenatal diagnosis of Apert syndrome is reviewed. ...
http://www.ncbi.nlm.nih.gov/pubmed/9263565
www.ncbi.nlm.nih.gov
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Beckwith-Wiedemann syndrome - Wikipedia, the free encyclopedia
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Exomphalos-macroglossia-gigantism syndrome in Jamaican infants" ... (Apert syndrome/Pfeiffer syndrome, Saethre-Chotzen syndrome, Carpenter syndrome, ...
http://en.wikipedia.org/wiki/Beckwith-Wiedemann_syndrome
en.wikipedia.org
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