X-linked hypohidrotic ectodermal dysplasia (XLHED): Clinical and diagnostic insights from an international patient registry

American Journal of Medical Genetics, Part A

Volumn 164, Issue 10, 2014, Pages 2437-2442

  Fete, Mary ^a   Hermann, Julie ^b   Behrens, Jeffrey ^b   Huttner, Kenneth M ^b  

^a National Foundation for Ectodermal Dysplasia   (United States)

^b Edimer Pharmaceuticals Inc   (United States)

Author keywords

Ectodermal dysplasias; Patient advocacy group; Registry; XLHED

Indexed keywords

ADOLESCENT; ADULT; AGE; DATA ANALYSIS; DISEASE REGISTRY; DISEASE SEVERITY; ECZEMA; FAILURE TO THRIVE; FAMILY HISTORY; FEEDING DIFFICULTY; FEMALE; GEOGRAPHIC DISTRIBUTION; HAIR DISEASE; HAIR LOSS; HOARSENESS; HUMAN; HYPODONTIA; HYPOHIDROTIC ECTODERMAL DYSPLASIA; MAJOR CLINICAL STUDY; MALE; NOSE OBSTRUCTION; PHENOTYPE; POPULATION RESEARCH; REVIEW; SEX DIFFERENCE; SINUSITIS; SWEATING; UNDERWEIGHT; VOICE CHANGE; WHEEZING; X LINKED HYPOHIDROTIC ECTODERMAL DYSPLASIA; COMPLICATION; ECTODERMAL DYSPLASIA; GENETIC DISEASES, X-LINKED; GENETICS; REGISTER;

ECTODYSPLASIN A;

ECTODERMAL DYSPLASIA; ECTODYSPLASINS; GENETIC DISEASES, X-LINKED; HUMANS; REGISTRIES;

EID: 84908253590     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.36436     Document Type: Review

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