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A case of Adams-Oliver Syndrome

MANIKANDASAMY V .

Abstract


A late preterm, 2.3kg, Male child was born to P2L2 mother by Normal Vaginal Delivery. Baby had a large scalp defect, acrania with hypoplastic and absent digits. Acrania portion of the skull was covered by a thick membrane. X-ray skull showed absence of skull vault, X-ray of extremities showed hypoplastic and absent digits. Neurosonogram was normal. Echocardiography done showed moderate PDA with left to right shunt. CT brain was normal. Child was diagnosed as a case of Adams Oliver syndrome. It is an autosomal dominant disorder comprises aplasia cutis congenita with terminal transverse limb defects.


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References


Whitely CB, Gorlin RJ. Adams Oliver Revisited. American Journal ofMedical genetics 1991: 40: 319-26.

Bamforth JS, Kaurah P, Byrne J, Ferreira P. Adams Oliver Syndrome: Afamily with variability in clinical expression. American Journal of Medicalgenetics 1994: 49: 393-96.

Smith’s recognizable patterns of human malformations 7th edition. P 416.


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