Schöpf-Schulz-Passarge syndrome: Further delineation of the phenotype and genetic considerations

Acta Dermato-Venereologica

Volumn 88, Issue 6, 2008, Pages 607-612

  Castori, Marco ^a   Ruggieri, Salvatore ^a   Giannetti, Luca ^b   Annessi, Giorgio ^a   Zambruno, Giovanna ^a  

^a LABORATORIO DI PATOLOGIA VASCOLARE   (Italy)

^b UNIVERSITY OF MODENA AND REGGIO EMILIA   (Italy)

Author keywords

Autosomal recessive; Ectodermal dysplasia; Genodermatosis; Skin appendages; Tricho odonto onycho dermal dysplasia; Tumour predisposition

Indexed keywords

AGED; AGING; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; BREAST HYPOPLASIA; CANCER RISK; CASE REPORT; CLINICAL FEATURE; CONSANGUINEOUS MARRIAGE; DISEASE COURSE; ECTODERMAL DYSPLASIA; EYELID TUMOR; FEMALE; GENE LOCUS; GENETIC HETEROGENEITY; GENODERMATOSIS; HIDRADENOMA; HUMAN; MALE; MUTATIONAL ANALYSIS; OPTIC NERVE ATROPHY; PATIENT REFERRAL; PEDIGREE ANALYSIS; PHYSICAL EXAMINATION; PRIORITY JOURNAL; SCHOPF SCHULZ PASSARGE SYNDROME; SIBLING; SKIN BIOPSY; SKIN EXAMINATION; SWEAT GLAND TUMOR;

AGED; ANODONTIA; CONSANGUINITY; ECTODERMAL DYSPLASIA; EYELID NEOPLASMS; FEMALE; HIDROCYSTOMA; HUMANS; HYPOTRICHOSIS; KERATODERMA, PALMOPLANTAR; MALE; NAILS, MALFORMED; NIPPLES; OPTIC ATROPHY; PHENOTYPE; SWEAT GLAND NEOPLASMS; SYNDROME;

EID: 56749144138     PISSN: 00015555     EISSN: None     Source Type: Journal    
DOI: 10.2340/00015555-0547     Document Type: Article

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