About: Schöpf–Schulz–Passarge syndrome

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Schöpf–Schulz–Passarge syndrome is an autosomal recessive condition with punctate symmetric palmoplantar keratoderma, with the keratoderma and fragility of the nails beginning around age 12. In addition to palmoplantar keratoderma, other symptoms include hypodontia, hypotrichosis, nail dystrophies, and eyelid cysts (apocrine hidrocystomas). Patients may also develop syringofibroadenoma and squamous cell carcinomas. It was characterized in 1971. It has been associated with WNT10A.

Attributes	Values
rdf:type	Thing Disease yago:WikicatPalmoplantarKeratodermas yago:Abstraction100002137 yago:Attribute100024264 yago:Condition113920835 yago:Disease114070360 yago:IllHealth114052046 yago:Illness114061805 yago:Keratoderma114227906 yago:PathologicalState114051917 yago:PhysicalCondition114034177 disease yago:SkinDisease114219661 yago:State100024720
rdfs:label	Schöpf-Schulz-Passarge-Syndrom (de) Schöpf–Schulz–Passarge syndrome (en)
rdfs:comment	Schöpf–Schulz–Passarge syndrome is an autosomal recessive condition with punctate symmetric palmoplantar keratoderma, with the keratoderma and fragility of the nails beginning around age 12. In addition to palmoplantar keratoderma, other symptoms include hypodontia, hypotrichosis, nail dystrophies, and eyelid cysts (apocrine hidrocystomas). Patients may also develop syringofibroadenoma and squamous cell carcinomas. It was characterized in 1971. It has been associated with WNT10A. (en) Das Schöpf-Schulz-Passarge-Syndrom (SSPS) ist eine sehr seltene angeborene Hauterkrankung (Genodermatose) und wird sowohl zu den Hereditären Palmoplantarkeratosen als auch zur Ektodermalen Dysplasie gezählt. Zusätzliche Hauptmerkmale sind ekkrine Tumoren, Zysten der Augenlider, Störungen der Zahnanlagen (Hypodontie) und der Körperbehaarung (Hypotrichose). Synonyme sind: Schöpf-Syndrom; Palmoplantare ektodermale Dysplasie Typ XXIX; englisch Keratosis Palmoplantaris With Cystic Eyelids, Hypodontia, And Hypotrichosis; Eccrine Tumors With Ectodermal Dysplasia (de)
foaf:name	Schöpf–Schulz–Passarge syndrome (en)
name	Schöpf–Schulz–Passarge syndrome (en)
dcterms:subject	Syndromes Palmoplantar keratodermas
Wikipage page ID	21522840 (xsd:integer)
Wikipage revision ID	993079438 (xsd:integer)
Link from a Wikipage to another Wikipage	List of cutaneous neoplasms associated with systemic syndromes List of dental abnormalities associated with cutaneous conditions Hypodontia Autosomal recessive Palmoplantar keratoderma Hypotrichosis Syndromes Palmoplantar keratodermas Apocrine hidrocystoma Syringofibroadenoma WNT10A List of cutaneous conditions Squamous cell carcinoma
sameAs	Schöpf–Schulz–Passarge syndrome Schöpf–Schulz–Passarge syndrome Schöpf–Schulz–Passarge syndrome Schöpf–Schulz–Passarge syndrome Schöpf–Schulz–Passarge syndrome
dbp:wikiPageUsesTemplate	dbt:Infobox_medical_condition_(new) dbt:Medical_resources dbt:Reflist dbt:Rp dbt:Cutaneous-condition-stub
ICD	(en) Q82.8 (en)
OMIM	224750 (xsd:integer)
synonyms	Eyelid cysts, Palmoplantar keratoderma, Hypodontia, and Hypotrichosis (en)
has abstract	Das Schöpf-Schulz-Passarge-Syndrom (SSPS) ist eine sehr seltene angeborene Hauterkrankung (Genodermatose) und wird sowohl zu den Hereditären Palmoplantarkeratosen als auch zur Ektodermalen Dysplasie gezählt. Zusätzliche Hauptmerkmale sind ekkrine Tumoren, Zysten der Augenlider, Störungen der Zahnanlagen (Hypodontie) und der Körperbehaarung (Hypotrichose). Synonyme sind: Schöpf-Syndrom; Palmoplantare ektodermale Dysplasie Typ XXIX; englisch Keratosis Palmoplantaris With Cystic Eyelids, Hypodontia, And Hypotrichosis; Eccrine Tumors With Ectodermal Dysplasia Die Bezeichnung bezieht sich auf die Erstautoren der Erstbeschreibung aus dem Jahre 1971 durch den deutschen Hautarzt und Humangenetiker Erwin Schöpf, H.-J. Schulz und Eberhard Passarge. (de) Schöpf–Schulz–Passarge syndrome is an autosomal recessive condition with punctate symmetric palmoplantar keratoderma, with the keratoderma and fragility of the nails beginning around age 12. In addition to palmoplantar keratoderma, other symptoms include hypodontia, hypotrichosis, nail dystrophies, and eyelid cysts (apocrine hidrocystomas). Patients may also develop syringofibroadenoma and squamous cell carcinomas. It was characterized in 1971. It has been associated with WNT10A. (en)
gold:hypernym	Condition
prov:wasDerivedFrom	wikipedia-en:Schöpf–Schulz–Passarge_syndrome?oldid=993079438&ns=0
page length (characters) of wiki page	3086 (xsd:nonNegativeInteger)
ICD10	Q82.8
OMIM id	224750 (xsd:integer)
foaf:isPrimaryTopicOf	wikipedia-en:Schöpf–Schulz–Passarge_syndrome
is Link from a Wikipage to another Wikipage of	Schopf-Schulz-Passarge syndrome List of cutaneous neoplasms associated with systemic syndromes List of dental abnormalities associated with cutaneous conditions Keratoderma List of OMIM disorder codes Howel–Evans syndrome Schöpf-Schulz-Passarge syndrome Eyelid cysts, palmoplantar keratoderma, hypodontia, and hypotrichosis Eyelid cysts with palmoplantar keratoderma and hypodontia and hypotrichosis List of skin conditions List of syndromes WNT10A Schopf–Schulz–Passarge syndrome
is Wikipage redirect of	Schopf-Schulz-Passarge syndrome Schöpf-Schulz-Passarge syndrome Eyelid cysts, palmoplantar keratoderma, hypodontia, and hypotrichosis Eyelid cysts with palmoplantar keratoderma and hypodontia and hypotrichosis Schopf–Schulz–Passarge syndrome
is foaf:primaryTopic of	wikipedia-en:Schöpf–Schulz–Passarge_syndrome

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