Document Detail


Clinical lessons learned from the International Research Symposium on Ankyloblepharon-Ectodermal Defects-Cleft Lip/Palate (AEC) syndrome.
MedLine Citation:
PMID:  19676057     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The International Research Symposium on Ankyloblepharon-Ectodermal Defects-Cleft Lip/Palate ((AEC) Syndrome, that was supported by the National Foundation for Ectodermal Dysplasias (NFED) through a grant from the National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) and the National Institutes of Health Office of Rare Diseases (NIH-ORD), brought together physicians, scientists, and 23 individuals affected by AEC syndrome from 13 families. Eighteen of the AEC-affected individuals were enrolled in an IRB-approved protocol through Baylor College of Medicine. Enrolled participants had clinical evaluations by multiple subspecialists, and additionally submitted blood for mutational analysis and skin specimens for pathologic evaluation. One of the goals of the conference was to define clinical and pathologic findings for improved diagnostic criteria, with the hope of determining genotype-phenotype correlations that might aid in predicting prognosis or directing therapeutics. What we found was wide interfamilial and intrafamilial variability in the manifestations of the syndrome. We were unable to identify any specific genotype-phenotype correlations. This may relate to our small sample size or other unknown epigenetic factors that are also at play in the expression and manifestation of the syndrome in specific individuals.
Authors:
Alanna F Bree
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  American journal of medical genetics. Part A     Volume:  149A     ISSN:  1552-4833     ISO Abbreviation:  Am. J. Med. Genet. A     Publication Date:  2009 Sep 
Date Detail:
Created Date:  2009-08-26     Completed Date:  2010-01-05     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  101235741     Medline TA:  Am J Med Genet A     Country:  United States    
Other Details:
Languages:  eng     Pagination:  1894-9     Citation Subset:  IM    
Copyright Information:
(c) 2009 Wiley-Liss, Inc.
Affiliation:
Department of Pediatric Dermatology, Texas Children's Hospital, Baylor College of Medicine, 6621 Fannin Street CC 620.16, Houston, TX 77030, USA. afbree@bcm.tmc.edu
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MeSH Terms
Descriptor/Qualifier:
Abnormalities, Multiple* / diagnosis,  genetics,  pathology
Adolescent
Adult
Child
Child, Preschool
Cleft Lip / diagnosis,  genetics,  pathology*
Cleft Palate / diagnosis,  genetics,  pathology*
Ectodermal Dysplasia* / diagnosis,  genetics,  pathology
Eyelids / abnormalities*
Face / pathology
Family
Female
Foot / pathology
Hand / pathology
Humans
Infant
Male
Mutation
Scalp / pathology
Siblings
Syndrome
Trans-Activators / genetics
Tumor Suppressor Proteins / genetics
Young Adult
Chemical
Reg. No./Substance:
0/TP63 protein, human; 0/Trans-Activators; 0/Tumor Suppressor Proteins

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