An Entity of Type: disease, from Named Graph: http://dbpedia.org, within Data Space: dbpedia.org

Hypotrichosis–lymphedema–telangiectasia syndrome is a congenital syndrome characterized by lymphedema (swelling of tissue due to malformation or malfunction of lymphatics), the presence of telegiectasias (small dilated vessels near the surface of the skin), and hypotrichosis or alopecia (hair loss). Lymphedema usually develops in the lower extremities during puberty. Hair is normal at birth, but usually lost during infancy. Telangiectasias may present on the palms and soles more commonly than on the scalp, legs, and genitalia. The syndrome has been reported in association with both autosomal dominant and autosomal recessive inheritance patterns.

Property Value
dbo:abstract
  • Hypotrichosis–lymphedema–telangiectasia syndrome is a congenital syndrome characterized by lymphedema (swelling of tissue due to malformation or malfunction of lymphatics), the presence of telegiectasias (small dilated vessels near the surface of the skin), and hypotrichosis or alopecia (hair loss). Lymphedema usually develops in the lower extremities during puberty. Hair is normal at birth, but usually lost during infancy. Telangiectasias may present on the palms and soles more commonly than on the scalp, legs, and genitalia. The syndrome has been reported in association with both autosomal dominant and autosomal recessive inheritance patterns. It is associated with a rare mutation of the transcription factor gene SOX18. (en)
dbo:meshId
  • C564327
dbo:omim
  • 607823 (xsd:integer)
dbo:wikiPageID
  • 30670029 (xsd:integer)
dbo:wikiPageLength
  • 3523 (xsd:nonNegativeInteger)
dbo:wikiPageRevisionID
  • 1106108685 (xsd:integer)
dbo:wikiPageWikiLink
dbp:meshid
  • 564327.0
dbp:name
  • Hypotrichosis–lymphedema–telangiectasia syndrome (en)
dbp:omim
  • 607823 (xsd:integer)
dbp:synonyms
  • Hypotrichosis-lymphedema-telangiectasia-membranoproliferative glomerulonephritis syndrome (en)
dbp:wikiPageUsesTemplate
dcterms:subject
gold:hypernym
rdf:type
rdfs:comment
  • Hypotrichosis–lymphedema–telangiectasia syndrome is a congenital syndrome characterized by lymphedema (swelling of tissue due to malformation or malfunction of lymphatics), the presence of telegiectasias (small dilated vessels near the surface of the skin), and hypotrichosis or alopecia (hair loss). Lymphedema usually develops in the lower extremities during puberty. Hair is normal at birth, but usually lost during infancy. Telangiectasias may present on the palms and soles more commonly than on the scalp, legs, and genitalia. The syndrome has been reported in association with both autosomal dominant and autosomal recessive inheritance patterns. (en)
rdfs:label
  • Hypotrichosis–lymphedema–telangiectasia syndrome (en)
owl:sameAs
prov:wasDerivedFrom
foaf:isPrimaryTopicOf
foaf:name
  • Hypotrichosis–lymphedema–telangiectasia syndrome (en)
is dbo:wikiPageRedirects of
is dbo:wikiPageWikiLink of
is foaf:primaryTopic of
Powered by OpenLink Virtuoso    This material is Open Knowledge     W3C Semantic Web Technology     This material is Open Knowledge    Valid XHTML + RDFa
This content was extracted from Wikipedia and is licensed under the Creative Commons Attribution-ShareAlike 3.0 Unported License