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

Acrocraniofacial dysostosis, also known as Kaplan Plauchu Fitch syndrome is a very rare hereditary disorder which is characterized by cranio-facial dysmorphisms, hearing loss, digital clubbing, and osseous anomalies. Only 2 cases have been described in medical literature.

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dbo:abstract
  • Acrocraniofacial dysostosis, also known as Kaplan Plauchu Fitch syndrome is a very rare hereditary disorder which is characterized by cranio-facial dysmorphisms, hearing loss, digital clubbing, and osseous anomalies. Only 2 cases have been described in medical literature. (en)
dbo:alias
  • (en)
  • Kaplan Plauchu Fitch syndrome (en)
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  • 70965503 (xsd:integer)
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  • 4012 (xsd:nonNegativeInteger)
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  • 1117556676 (xsd:integer)
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dbp:causes
  • Autosomal recessive inheritance (en)
dbp:deaths
  • - (en)
dbp:diagnosis
dbp:duration
  • Lifelong (en)
dbp:frequency
  • very rare, only 2 cases have been described in medical literature (en)
dbp:imageSize
  • 200 (xsd:integer)
dbp:name
  • Acrocraniofacial dysostosis (en)
dbp:onset
  • Conception (en)
dbp:prevention
  • None (en)
dbp:prognosis
  • Good (en)
dbp:specialty
dbp:synonyms
  • Kaplan Plauchu Fitch syndrome (en)
dbp:wikiPageUsesTemplate
dcterms:subject
rdf:type
rdfs:comment
  • Acrocraniofacial dysostosis, also known as Kaplan Plauchu Fitch syndrome is a very rare hereditary disorder which is characterized by cranio-facial dysmorphisms, hearing loss, digital clubbing, and osseous anomalies. Only 2 cases have been described in medical literature. (en)
rdfs:label
  • Acrocraniofacial dysostosis (en)
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