CASE REPORT: AGENESIS OF CORPUS CALLOUSUM

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RESHADAT S.

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Journal Paper

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Journal: SCIENTIFIC JOURNAL OF KURDISTAN UNIVERSITY OF MEDICAL SCIENCES Year:2008 | Volume:13 | Issue:2 (SERIAL NUMBER 48) Page(s): 87-93

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Title

CASE REPORT: AGENESIS OF CORPUS CALLOUSUM

Author(s)

RESHADAT S. | Issue Writer Certificate

Keywords

CORPUS CALLOUSUMQ2

METABOLIC DISORDERSQ3

Abstract

Background and Aim: Corpus callosum is the biggest cornisure of interventricula. The main etiology of agenesis of CORPUS CALLOUSUM is the failure of programmed cellular death. This disease comprises a heterogenic group of disorders which has a wide range of presentations frorn medical and neurological symptoms to asymptomatic patients with normal intelligence. Diagnosis of this disease can be made by use of CT and MRI. The disease can be transmitted via autosomal dominant or X-linked genes and can be associated with chromosomal disorders such as trisomy of 8 and 18 and different METABOLIC DISORDERS. There is no standard therapy for this disorder. Prognoses of the patients are variable and usually the disorder does not lead to death.Case report: The patient was admitted, for the first time, to the hospital when he was 3 day old because his mother had a sonography at the 28th week of pregnancy which was compatible with a cyst in the brain of her fetus. After delivery the parents of the patient referred to the pediatric clinic for further evaluation of their neonate. After examination of the patient and preclinical studies, the patient was diagnosed as a case of agenesis of CORPUS CALLOUSUM. Neurological examination of the patients was within norrnallimits. The growth indices of the patient were normal and there was no evidence of any neurological, metabolic or chromosomal disorders on clinical and preclinical grounds.Conclusion: Agenesis of corpus callosum is a rare disorder which can be associated with hypotonia, seizure, hydrocephalus, acidosis, hypoglycemia, hepatomegaly, increased serum ammonia, chromosomal disorders and ophthalmologic diseases such as cataract, optic nerve atrophy and... . But no evidence of any above- mentioned disorders was found in our patient on clinical and paraclincal grounds, which indicates a wide range of clinical signs and symptoms in this disorder.

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APA: Copy

RESHADAT, S.. (2008). CASE REPORT: AGENESIS OF CORPUS CALLOUSUM. SCIENTIFIC JOURNAL OF KURDISTAN UNIVERSITY OF MEDICAL SCIENCES, 13(2 (SERIAL NUMBER 48)), 87-93. SID. https://sid.ir/paper/76304/en

Vancouver: Copy

RESHADAT S.. CASE REPORT: AGENESIS OF CORPUS CALLOUSUM. SCIENTIFIC JOURNAL OF KURDISTAN UNIVERSITY OF MEDICAL SCIENCES[Internet]. 2008;13(2 (SERIAL NUMBER 48)):87-93. Available from: https://sid.ir/paper/76304/en

IEEE: Copy

S. RESHADAT, “CASE REPORT: AGENESIS OF CORPUS CALLOUSUM,” SCIENTIFIC JOURNAL OF KURDISTAN UNIVERSITY OF MEDICAL SCIENCES, vol. 13, no. 2 (SERIAL NUMBER 48), pp. 87–93, 2008, [Online]. Available: https://sid.ir/paper/76304/en

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