Volume 44, Issue 6 pp. 786-789
Brief Clinical Report
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Delayed membranous cranial ossification in a mother and child

Ariadna Gonzalez-del Angel

Ariadna Gonzalez-del Angel

Department of Genetics, Instituto Nacional de Pediatría, Mexico D.F., México

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Dra. Alessandra Carnevale

Corresponding Author

Dra. Alessandra Carnevale

Department of Genetics, Instituto Nacional de Pediatría, Mexico D.F., México

Departamento de Genética, Instituto Nacional de Pediatría, Insurgentes Sur 3700 C., México D.F. 04530, MéxicoSearch for more papers by this author
Raul Takenaga

Raul Takenaga

Department of Radiology, Instituto Nacional de Pediatría, Mexico D.F., México

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First published: 1 December 1992
Citations: 5

Abstract

We report on a girl and her mother with delayed intramembranous ossification of the cranial vault. The 11-month-old girl had a large ossification defect involving parietal bones, squamous portion of temporal bones, and interparietal region of occipital bone, while the mother showed a complete ossified cranial vault with flat posterior parietal region and prominent occiput. Both had a similar face characterized by frontal bossing, hypertelorism, downward slant of palpebral fissures, flat nasal bridge, and short midface. On reviewing the literature, we concluded that these cases may be a dominant transmitted ossification defect with characteristic face, different from the cranium bifidum-parietal foramina entity. © 1992 Wiley-Liss, Inc.

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