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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Published in: | Child's nervous system Vol. 22; no. 6; pp. 632 - 634 |
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Main Authors: | , , , |
Format: | Journal Article |
Language: | English |
Published: |
Germany
01-06-2006
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Subjects: | |
Online Access: | Get full text |
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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. |
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Bibliography: | ObjectType-Case Study-2 SourceType-Scholarly Journals-1 ObjectType-Feature-4 content type line 23 ObjectType-Report-1 ObjectType-Article-3 |
ISSN: | 0256-7040 1433-0350 |
DOI: | 10.1007/s00381-005-0041-z |