rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
5
|
pubmed:dateCreated |
1990-7-17
|
pubmed:abstractText |
The observation of two new cases in a previously reported family has brought about a change in the delineation of the syndrome initially defined. To the abnormalities already described (branchial dysplasia, mental deficiency, club feet, inguinal herniae) must be added a paucity of interlobular bile duts; the relationship between this new syndrome and the Alagille syndrome requires reconsideration.
|
pubmed:commentsCorrections |
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
|
pubmed:month |
May
|
pubmed:issn |
0022-2593
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:volume |
27
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
330-2
|
pubmed:dateRevised |
2011-11-17
|
pubmed:meshHeading |
pubmed-meshheading:2352262-Biliary Atresia,
pubmed-meshheading:2352262-Foot Deformities, Congenital,
pubmed-meshheading:2352262-Genes, Recessive,
pubmed-meshheading:2352262-Hernia, Inguinal,
pubmed-meshheading:2352262-Humans,
pubmed-meshheading:2352262-Infant,
pubmed-meshheading:2352262-Intellectual Disability,
pubmed-meshheading:2352262-Male,
pubmed-meshheading:2352262-Syndrome
|
pubmed:year |
1990
|
pubmed:articleTitle |
Branchial dysplasia, mental deficiency, club feet, and inguinal herniae: a report of two further cases associated with paucity of interlobular bile ducts.
|
pubmed:affiliation |
Unité de Génétique Médicale, Hôpital de Cimiez, Nice, France.
|
pubmed:publicationType |
Journal Article,
Comparative Study,
Case Reports
|