303494

Source:http://linkedlifedata.com/resource/pubmed/id/303494

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0039082, umls-concept:C0241888
pubmed:issue	6-7
pubmed:dateCreated	1977-12-29
pubmed:abstractText	The François' syndrome associates disseminated firm nodular subcutaneous lesions, a deforming arthropathy and a corneal dystrophy. Inheritance seems to be recessive. Six cases of this rare syndrome have been previously published. The syndrome is reported here in two Mexican brothers. In the authors' opinion the François' syndrome is not related to the xanthomatoses. It should be considered as a genetically recessive arthropathic nodular fibromatosis.
pubmed:language	fre
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7702013
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:issn	0151-9638
pubmed:author	pubmed-author:Ruiz-MaldonadoRR, pubmed-author:TamayoLL, pubmed-author:VelazquezEE
pubmed:issnType	Print
pubmed:volume	104
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	475-8
pubmed:dateRevised	2006-11-15
pubmed:meshHeading	pubmed-meshheading:303494-Child, pubmed-meshheading:303494-Child, Preschool, pubmed-meshheading:303494-Corneal Dystrophies, Hereditary, pubmed-meshheading:303494-Exostoses, Multiple Hereditary, pubmed-meshheading:303494-Female, pubmed-meshheading:303494-Humans, pubmed-meshheading:303494-Male, pubmed-meshheading:303494-Skin Diseases, pubmed-meshheading:303494-Syndrome
pubmed:articleTitle	[Familial dermo-chondro-corneal dystrophy (François' syndrome)].
pubmed:publicationType	Journal Article, English Abstract, Case Reports