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Abetalipoproteinemia in a Saudi infant
JCPSP-Journal of the College of Physicians and Surgeons Pakistan. 2011; 21 (2): 117-118
in En | IMEMR | ID: emr-103678
Responsible library: EMRO
ABSTRACT
Abetalipoproteinemia is a rare genetic disorder. A 5-month-old Saudi boy presented with chronic diarrhoea and failure to thrive since 3 months of age. He was cachectic. His peripheral blood picture showed many acanthocytes and he had very low lipid profile. He improved on medium chain triglyceride [MCT] formula and administration of fat soluble vitamins
Subject(s)
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Index: IMEMR Main subject: Cachexia / Chronic Disease / Diarrhea, Infantile / Failure to Thrive / Acanthocytes / Infant Type of study: Case_reports Limits: Humans / Male Language: En Journal: J. Coll. Physicians Surg. Pak. Year: 2011
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Index: IMEMR Main subject: Cachexia / Chronic Disease / Diarrhea, Infantile / Failure to Thrive / Acanthocytes / Infant Type of study: Case_reports Limits: Humans / Male Language: En Journal: J. Coll. Physicians Surg. Pak. Year: 2011