Chiari I malformation and idiopathic growth hormone deficiency in siblings

The authors report a case of three brothers. Two of these siblings presented with congenital growth hormone deficiency and Chiari I malformation. The third and younger brother has been found not to have growth hormone deficiency or the Chiari I malformation. Sparse cases of these two clinical occurr...

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Bibliographic Details
Published in:Child's nervous system Vol. 22; no. 6; pp. 632 - 634
Main Authors: Murphy, R L, Tubbs, R S, Grabb, P A, Oakes, W J
Format: Journal Article
Language:English
Published: Germany 01-06-2006
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Summary:The authors report a case of three brothers. Two of these siblings presented with congenital growth hormone deficiency and Chiari I malformation. The third and younger brother has been found not to have growth hormone deficiency or the Chiari I malformation. Sparse cases of these two clinical occurrences have been reported. Further, the posterior cranial fossa has been determined to be altered in patients with Chiari I malformation and growth hormone deficiency. Our current case reports strengthen the association between these two pathological entities and are, to our knowledge, the first description of both defects in siblings.
Bibliography:ObjectType-Case Study-2
SourceType-Scholarly Journals-1
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ISSN:0256-7040
1433-0350
DOI:10.1007/s00381-005-0041-z