Occipital horn syndrome - Additional radiographic findings in two new cases

T. E. Herman; W. H. McAlister; A. Boniface; M. P. Whyte

doi:10.1007/BF02016258

Occipital horn syndrome - Additional radiographic findings in two new cases

T. E. Herman, W. H. McAlister, A. Boniface, M. P. Whyte

Section of Pediatric Radiology

Research output: Contribution to journal › Article › peer-review

13 Scopus citations

Abstract

Occipital horn syndrome, a rare genetic disorder of copper metabolism, was recognized in 2 unrelated patients. Radiographs of these patients at various ages allowed confirmation of previously described radiographic findings. In addition, new radiographic manifestations were encountered. These pathognomonic radiographic findings are presented and the clinical and biochemical features of occipital horn syndrome are reviewed.

Original language	English
Pages (from-to)	363-365
Number of pages	3
Journal	Pediatric radiology
Volume	22
Issue number	5
DOIs	https://doi.org/10.1007/BF02016258
State	Published - Sep 1992

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10.1007/BF02016258

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@article{0f6df6d5fa9847a5910f808464d94bbe,

title = "Occipital horn syndrome - Additional radiographic findings in two new cases",

abstract = "Occipital horn syndrome, a rare genetic disorder of copper metabolism, was recognized in 2 unrelated patients. Radiographs of these patients at various ages allowed confirmation of previously described radiographic findings. In addition, new radiographic manifestations were encountered. These pathognomonic radiographic findings are presented and the clinical and biochemical features of occipital horn syndrome are reviewed.",

author = "Herman, {T. E.} and McAlister, {W. H.} and A. Boniface and Whyte, {M. P.}",

year = "1992",

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doi = "10.1007/BF02016258",

language = "English",

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pages = "363--365",

journal = "Pediatric radiology",

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T1 - Occipital horn syndrome - Additional radiographic findings in two new cases

AU - Herman, T. E.

AU - McAlister, W. H.

AU - Boniface, A.

AU - Whyte, M. P.

PY - 1992/9

Y1 - 1992/9

N2 - Occipital horn syndrome, a rare genetic disorder of copper metabolism, was recognized in 2 unrelated patients. Radiographs of these patients at various ages allowed confirmation of previously described radiographic findings. In addition, new radiographic manifestations were encountered. These pathognomonic radiographic findings are presented and the clinical and biochemical features of occipital horn syndrome are reviewed.

AB - Occipital horn syndrome, a rare genetic disorder of copper metabolism, was recognized in 2 unrelated patients. Radiographs of these patients at various ages allowed confirmation of previously described radiographic findings. In addition, new radiographic manifestations were encountered. These pathognomonic radiographic findings are presented and the clinical and biochemical features of occipital horn syndrome are reviewed.

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U2 - 10.1007/BF02016258

DO - 10.1007/BF02016258

M3 - Article

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AN - SCOPUS:0026671327

SN - 0301-0449

VL - 22

SP - 363

EP - 365

JO - Pediatric radiology

JF - Pediatric radiology

IS - 5

ER -

Occipital horn syndrome - Additional radiographic findings in two new cases

Abstract

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