Schopf–Schulz–Passarge syndrome

Schopf–Schulz–Passarge syndrome

Schopf–Schulz–Passarge syndrome (SSPS) is a rare type of ectodermal dysplasia that has autosomal recessive inheritance. It is characterized by palmoplantar keratoderma, hypodontia, hypotrichosis, nail dystrophy, and multiple periocular and eyelid apocrine hidrocystomas. A 36-year-old male presented...

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Bibliographic Details
Main Authors: Kinjal D Rambhia, Vidya Kharkar, Sunanda Mahajan, Uday S Khopkar
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2018-01-01
Series:Indian Dermatology Online Journal
Subjects:
Apocrine hidrocystomas
ectodermal dysplasia
keratoderma
Schopf–Schulz–Passarge syndrome
Online Access:http://www.idoj.in/article.asp?issn=2229-5178;year=2018;volume=9;issue=6;spage=448;epage=451;aulast=Rambhia

Internet

http://www.idoj.in/article.asp?issn=2229-5178;year=2018;volume=9;issue=6;spage=448;epage=451;aulast=Rambhia

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