The group of epidermal nevus syndromes. Part I. Well defined phenotypes

Journal of the American Academy of Dermatology

Volumn 63, Issue 1, 2010, Pages 1-22

  Happle, Rudolf ^a  

^a PHILIPPS UNIVERSITY MARBURG   (Germany)

Author keywords

functional mosaicism of an X linked dominant, male lethal mutation; keratinocytic nevi; mosaicism of autosomal lethal mutations; organiod nevi; paradominant inheritance; type 2 segmental Cowden disease

Indexed keywords

FIBROBLAST GROWTH FACTOR RECEPTOR 3; VITAMIN D;

ANGORA HAIR NEVUS; ANGORA HAIR NEVUS SYNDROME; BECKER NEVUS; CLINICAL FEATURE; COWDEN SYNDROME; GENETIC RISK; GENETIC TRAIT; HUMAN; INHERITANCE; KERATINOCYTIC NEVUS; LEARNING; MULTIPLE CANCER; NEVUS; NEVUS COMEDONICUS; NEVUS COMEDONICUS SYNDROME; PHACOMATOSIS PIGMENTOKERATOTICA; PHENOTYPE; PRIORITY JOURNAL; REVIEW; RICKETS; SCHIMMELPENNING SYNDROME; SEBACEOUS NEVUS;

CHILD; CHILD, PRESCHOOL; FEMALE; HAMARTOMA SYNDROME, MULTIPLE; HUMANS; INFANT; INFANT, NEWBORN; MALE; NEUROCUTANEOUS SYNDROMES; NEVUS; NEVUS, SEBACEOUS OF JADASSOHN; PHENOTYPE; PROTEUS SYNDROME; SKIN NEOPLASMS; SYNDROME;

EID: 77953245900     PISSN: 01909622     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jaad.2010.01.017     Document Type: Review

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