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ID

http://id.who.int/icd/entity/441760957

Preferred Name

Syndrome de Schöpf-Schulz-Passarge

Definitions

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

Type

http://www.w3.org/2002/07/owl#Class

comment

Le syndrome de Schöpf-Schulz-Passarge (SSPS) est une dysplasie ectodermique rare à transmission autosomique récessive caractérisée par des hidrocystomes apocrines multiples des paupières, une kératodermie palmoplantaire, une hypotrichose, une hypodontie et une dystrophie des ongles.

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

schöpf-schulz-passarge σύνδρομο (ssps) είναι ένα σπάνιο autosomal υπολειπόμενο υπολειπόμενο εκφυλισμό που χαρακτηρίζεται από πολλαπλή οπίσθια απόκρυφη hidrocystomas, palmoplantar keratoderma, hypotrichosis, hypodontia και δυστροφία των νυχιών.

zespół schöpf-schulz-passarge (ssps) jest rzadką autosomalną dysplazją ektodermalną, charakteryzującą się licznymi hidrocystomami powiek, palmoplantar keratoderma, hipotrichosis, hypodontia i paznokci dystrophy.

schöpf-schulz-passarge-Syndrom (ssps) ist eine seltene autosomal rezessive ektodermale Dysplasie, die durch multiples apokrines Hidrozytom der Augenlider, palmoplantäre Keratodermie, Hypotrichose, Hypodontie und Nageldystrophie gekennzeichnet ist.

broaderTransitive

http://id.who.int/icd/entity/1156567558

http://id.who.int/icd/entity/2088802678

http://id.who.int/icd/entity/595701953

http://id.who.int/icd/entity/264268169

prefLabel

Syndrome de Schöpf-Schulz-Passarge

browserUrl

NA

label

Syndrome de Schöpf-Schulz-Passarge

νατρίου fluoroacetate

Schöpf-Schulz-Passarge syndrome

schöpf-schulz-passarge-Syndrom

zespół schöpf-schulz-passarge

subClassOf

http://id.who.int/icd/entity/1156567558

http://id.who.int/icd/entity/264268169

http://id.who.int/icd/entity/2088802678

http://id.who.int/icd/entity/595701953

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