Linked Life Data

2469415

Source:http://linkedlifedata.com/resource/pubmed/id/2469415

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
1989-6-7
pubmed:abstractText
To our knowledge, this is the third (possibly the fourth) description of a family with partial aplasia of the cerebellar vermis. The major clinical features are normal intelligence, delayed achievement of motor milestones, truncal ataxia, and nystagmus. Twelve of 14 affected individuals are female. The two affected males were more severely affected than were their female relatives. These findings along with apparently increased fetal wastage suggest that an X-linked rather than an autosomal dominant mode of inheritance may be responsible for this disorder.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
0003-9942
pubmed:author
pubmed:issnType
Print
pubmed:volume
46
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
582-3
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed:year
1989
pubmed:articleTitle
Familial aplasia of the cerebellar vermis. Possible X-linked dominant inheritance.
pubmed:affiliation
Department of Neurology, Vanderbilt University Medical Center, Nashville, Tenn.
pubmed:publicationType
Journal Article, Case Reports