Clinical and genetic heterogeneity in keratosis follicularis spinulosa decalvans

European Journal of Medical Genetics

Volumn 52, Issue 1, 2009, Pages 53-58

  Castori, Marco ^a   Covaciu, Claudia ^a   Paradisi, Mauro ^a   Zambruno, Giovanna ^a  

^a LABORATORIO DI PATOLOGIA VASCOLARE   (Italy)

Author keywords

Aminoaciduria; Autosomal dominant; Contiguous gene syndrome; Siemens 1 syndrome; X linked

Indexed keywords

ADULT; ALOPECIA; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CASE REPORT; CHILD; DENTAL CARIES; ENAMEL HYPOPLASIA; ERYTHEMA; EYE DISEASE; FAMILY; FOLLICULITIS; GENETIC HETEROGENEITY; GENODERMATOSIS; HUMAN; INFLAMMATION; KERATODERMA; KERATOSIS; KERATOSIS FOLLICULARIS SPINULOSA; KERATOSIS PILARIS; MALE; MEDICAL LITERATURE; NAIL DISEASE; NAIL DYSTROPHY; PRESCHOOL CHILD; SCAR ALOPECIA; X CHROMOSOME LINKED DISORDER;

ABNORMALITIES, MULTIPLE; ALOPECIA; DARIER DISEASE; FAMILY HEALTH; FEMALE; GENETIC DISEASES, X-LINKED; HUMANS; LINKAGE (GENETICS); MALE; PEDIGREE; PHOTOPHOBIA;

EID: 58149123624     PISSN: 17697212     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ejmg.2008.09.005     Document Type: Article

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