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Delayed membranous cranial ossification in a mother and child.
Am J Med Genet. 1992 Dec 01; 44(6):786-9.AJ

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.

Authors+Show Affiliations

Department of Genetics, Instituto Nacional de Pediatría, Mexico, D.F.No affiliation info availableNo affiliation info available

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

1481847

Citation

Gonzalez-del Angel, A, et al. "Delayed Membranous Cranial Ossification in a Mother and Child." American Journal of Medical Genetics, vol. 44, no. 6, 1992, pp. 786-9.
Gonzalez-del Angel A, Carnevale A, Takenaga R. Delayed membranous cranial ossification in a mother and child. Am J Med Genet. 1992;44(6):786-9.
Gonzalez-del Angel, A., Carnevale, A., & Takenaga, R. (1992). Delayed membranous cranial ossification in a mother and child. American Journal of Medical Genetics, 44(6), 786-9.
Gonzalez-del Angel A, Carnevale A, Takenaga R. Delayed Membranous Cranial Ossification in a Mother and Child. Am J Med Genet. 1992 Dec 1;44(6):786-9. PubMed PMID: 1481847.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Delayed membranous cranial ossification in a mother and child. AU - Gonzalez-del Angel,A, AU - Carnevale,A, AU - Takenaga,R, PY - 1992/12/1/pubmed PY - 1992/12/1/medline PY - 1992/12/1/entrez SP - 786 EP - 9 JF - American journal of medical genetics JO - Am J Med Genet VL - 44 IS - 6 N2 - 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. SN - 0148-7299 UR - https://www.unboundmedicine.com/medline/citation/1481847/Delayed_membranous_cranial_ossification_in_a_mother_and_child_ L2 - https://onlinelibrary.wiley.com/resolve/openurl?genre=article&sid=nlm:pubmed&issn=0148-7299&date=1992&volume=44&issue=6&spage=786 DB - PRIME DP - Unbound Medicine ER -