Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
8
pubmed:dateCreated
1993-11-8
pubmed:abstractText
A mother and daughter are reported with apparently dissimilar syndromes. The mother has a split hand/split foot deformity and the daughter a condition consistent with a diagnosis of LADD syndrome. Absence of clefting and deficient formation of saliva and tears are the main signs that differentiate the LADD from the EEC syndrome. However, no distinct feature is constant between these two autosomal dominant disorders that show great phenotypic variability. This report emphasises the overlap between the LADD and the EEC syndromes.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/8411061-1415342, http://linkedlifedata.com/resource/pubmed/commentcorrection/8411061-1424230, http://linkedlifedata.com/resource/pubmed/commentcorrection/8411061-1741973, http://linkedlifedata.com/resource/pubmed/commentcorrection/8411061-1895319, http://linkedlifedata.com/resource/pubmed/commentcorrection/8411061-2222925, http://linkedlifedata.com/resource/pubmed/commentcorrection/8411061-3582415, http://linkedlifedata.com/resource/pubmed/commentcorrection/8411061-3709571, http://linkedlifedata.com/resource/pubmed/commentcorrection/8411061-4042394, http://linkedlifedata.com/resource/pubmed/commentcorrection/8411061-4078868, http://linkedlifedata.com/resource/pubmed/commentcorrection/8411061-4681851, http://linkedlifedata.com/resource/pubmed/commentcorrection/8411061-4725147, http://linkedlifedata.com/resource/pubmed/commentcorrection/8411061-4800520
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
0022-2593
pubmed:author
pubmed:issnType
Print
pubmed:volume
30
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
700-3
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed:year
1993
pubmed:articleTitle
Split hand/split foot deformity and LADD syndrome in a family: overlap between the EEC and LADD syndromes.
pubmed:affiliation
Department of Paediatrics and Medical Genetics, Pellegrin-Children's Hospital, Bordeaux, France.
pubmed:publicationType
Journal Article, Case Reports