Total: 3 |
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PMID (PMCID) | ||
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11446419 |
FEMALE | Child |
Adams-Oliver syndrome: further evidence for autosomal recessive inheritance. | ||
Unay B, Sarici SU, Gul D, Akin R, Gokcay E. Clin Dysmorphol. 2001;10(3):223-5. |
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We report a 7-year-old girl with Adams-Oliver syndrome who presented with extremely rare central nervous system anomalies including microcephaly, epilepsy, mental retardation and intracranial calcifications in addition to the classical scalp and limb defects. | ||
11233683 |
MALE | Infant, Newborn |
A case of Adams-Oliver syndrome associated with acrania, microcephaly, hemiplegia, epilepsy, and mental retardation. | ||
Caksen H, Kurtoglu S. Acta Neurol Belg. 2000;100(4):252-5. |
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A case of Adams-Oliver syndrome associated with acrania, microcephaly, hemiplegia, epilepsy, and mental retardation. | ||
8160731 |
FEMALE | Infant, Newborn |
Adams Oliver syndrome: a family with extreme variability in clinical expression. | ||
Bamforth JS, Kaurah P, Byrne J, Ferreira P. Am J Med Genet. 1994;49(4):393-6. |
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We describe a mother and her 3 children with variable scalp defects and limb defects consistent with a diagnosis of Adams Oliver syndrome also presenting with additional anomalies including congenital heart disease, microcephaly, epilepsy, mental retardation, arrhinencephaly, hydrocephaly, anatomic bronchial anomalies, and renal anomalies. |