Literature DB >> 8362912

Acalvaria: a unique congenital anomaly.

C P Harris1, J J Townsend, J C Carey.   

Abstract

Acalvaria is a rare malformation usually regarded as a postneurulation defect. It consists of absence of the calvarial bones, dura mater and associated muscles in the presence of a normal skull base and normal facial bones. The condition is frequently confused by prenatal ultrasonography with anencephaly or an encephalocele. Whereas the cerebral hemispheres are absent in anencephaly, the cranial contents in acalvaria are generally complete, though some neuropathological abnormality is often present. The presumed pathogenesis of acalvaria is faulty migration of the membranous neurocranium with normal placement of the embryonic ectoderm, resulting in absence of the calvaria but an intact layer of skin over the brain parenchyma. We describe 2 cases of acalvaria, one misdiagnosed ultrasonographically as an occipital encephalocele prenatally. The brain in one fetus demonstrated semilobar holoprosencephaly and micropolygyria, but in the other, was structurally and histologically normal with the exception of hydrocephalus.

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Year:  1993        PMID: 8362912     DOI: 10.1002/ajmg.1320460620

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  5 in total

1.  Fetal acalvaria with amniotic band syndrome.

Authors:  S Chandran; M K Lim; V Y Yu
Journal:  Arch Dis Child Fetal Neonatal Ed       Date:  2000-01       Impact factor: 5.747

2.  Meningocele following aplasia of the occipital bone.

Authors:  Torbjørn M Eggebø; Janne Brathetland; Hege U Dirdal; Gunnar Houge
Journal:  BMJ Case Rep       Date:  2011-02-17

3.  Acalvaria with external hydrocephalus: an uncommon case.

Authors:  Aldo Jose F da Silva
Journal:  Childs Nerv Syst       Date:  2018-08-02       Impact factor: 1.475

4.  Acalvaria: A rare congenital malformation.

Authors:  Vipul Gupta; Sunil Kumar
Journal:  J Pediatr Neurosci       Date:  2012-09

5.  Fetal MRI Characteristics of Exencephaly: A Case Report and Literature Review.

Authors:  Ali Sharif; Yihua Zhou
Journal:  Case Rep Radiol       Date:  2016-02-03
  5 in total

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