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A case of Adams-Oliver syndrome associated with acrania, microcephaly, hemiplegia, epilepsy, and mental retardation.
Acta Neurol Belg. 2000 Dec; 100(4):252-5.AN

Abstract

Adams-Oliver syndrome (AOS) is a rare congenital disorder, characterized by aplasia cutis congenita (ACC) of the scalp and variable degrees of terminal transverse limb defects. In this article, a newborn infant diagnosed as AOS for a large scalp defect, acrania, and finger malformations is presented. The patient was hospitalized and the scalp defect was successfully repaired with several surgical operations. During the hospitalization septicemia, meningitis, and convulsions developed, but they were successfully treated with appropriate antibiotics, antifungal, and anticonvulsive agents, He was discharged five months after admission to the hospital. Now, he is 3 years old, and has microcephaly, moderate mental retardation, left spastic hemiplegia, and epilepsy.

Authors+Show Affiliations

Department of Pediatrics, Yüzüncü Yil University Faculty of Medicine, Kayseri, Turkey.No affiliation info available

Pub Type(s)

Case Reports
Journal Article
Review

Language

eng

PubMed ID

11233683

Citation

Caksen, H, and S Kurtoğlu. "A Case of Adams-Oliver Syndrome Associated With Acrania, Microcephaly, Hemiplegia, Epilepsy, and Mental Retardation." Acta Neurologica Belgica, vol. 100, no. 4, 2000, pp. 252-5.
Caksen H, Kurtoğlu S. A case of Adams-Oliver syndrome associated with acrania, microcephaly, hemiplegia, epilepsy, and mental retardation. Acta Neurol Belg. 2000;100(4):252-5.
Caksen, H., & Kurtoğlu, S. (2000). A case of Adams-Oliver syndrome associated with acrania, microcephaly, hemiplegia, epilepsy, and mental retardation. Acta Neurologica Belgica, 100(4), 252-5.
Caksen H, Kurtoğlu S. A Case of Adams-Oliver Syndrome Associated With Acrania, Microcephaly, Hemiplegia, Epilepsy, and Mental Retardation. Acta Neurol Belg. 2000;100(4):252-5. PubMed PMID: 11233683.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - A case of Adams-Oliver syndrome associated with acrania, microcephaly, hemiplegia, epilepsy, and mental retardation. AU - Caksen,H, AU - Kurtoğlu,S, PY - 2001/3/10/pubmed PY - 2001/6/2/medline PY - 2001/3/10/entrez SP - 252 EP - 5 JF - Acta neurologica Belgica JO - Acta Neurol Belg VL - 100 IS - 4 N2 - Adams-Oliver syndrome (AOS) is a rare congenital disorder, characterized by aplasia cutis congenita (ACC) of the scalp and variable degrees of terminal transverse limb defects. In this article, a newborn infant diagnosed as AOS for a large scalp defect, acrania, and finger malformations is presented. The patient was hospitalized and the scalp defect was successfully repaired with several surgical operations. During the hospitalization septicemia, meningitis, and convulsions developed, but they were successfully treated with appropriate antibiotics, antifungal, and anticonvulsive agents, He was discharged five months after admission to the hospital. Now, he is 3 years old, and has microcephaly, moderate mental retardation, left spastic hemiplegia, and epilepsy. SN - 0300-9009 UR - https://www.unboundmedicine.com/medline/citation/11233683/A_case_of_Adams_Oliver_syndrome_associated_with_acrania_microcephaly_hemiplegia_epilepsy_and_mental_retardation_ DB - PRIME DP - Unbound Medicine ER -