Schöpf–Schulz–Passarge syndrome ^{الإنجليزية} (Q5679273)

SchC6pf-Schulz-Passarge syndrome (SSPS) is a rare autosomal recessive ectodermal dysplasia characterized by multiple eyelid apocrine hidrocystomas, palmoplantar keratoderma, hypotrichosis, hypodontia and nail dystrophy ^{الإنجليزية}

اللغة	التسمية	الوصف	أسماء أخرى
العربية	لم تُضف التسمية	لا يوجد وصف
الإنجليزية	Schöpf–Schulz–Passarge syndrome	SchC6pf-Schulz-Passarge syndrome (SSPS) is a rare autosomal recessive ectodermal dysplasia characterized by multiple eyelid apocrine hidrocystomas, palmoplantar keratoderma, hypotrichosis, hypodontia and nail dystrophy	Palmoplantar hyperkeratosis-cystic eyelids-hypodontia-hypotrichosis syndrome SSPS Palmoplantar keratoderma-cystic eyelids-hypodontia-hypotrichosis syndrome Schöpf-Schulz-Passarge syndrome Eccrine tumors-ectodermal dysplasia Eccrine Tumors With Ectodermal Dysplasia Keratosis Palmoplantaris With Cystic Eyelids, Hypodontia, and Hypotrichosis Keratosis palmoplantaris-cystic eyelids-hypodontia-hypotrichosis syndrome SCHOPF-SCHULZ-PASSARGE SYNDROME SCHOPF-SCHULZ-PASSARGE SYNDROME; SSPS Schopf-Schulz-Passarge syndrome

بيانات

Wikidata item ^{الإنجليزية}

Q7433355

٠ مرجع

وصلات الموقع

Marefa(٠ : لا وصلات)

ويكيبيديا(١ وصلة واحدة)

enwiki Schöpf–Schulz–Passarge syndrome