Middle East Journal of Digestive Diseases. 2015; 7 (3): 181-184
in English
| IMEMR
| ID: emr-166608
ABSTRACT
Abetalipoproteinemia [ABL] is a very rare autosomal recessive disorder caused by mutations in the microsomal triglyceride transfer protein gene [MTTP]. ABL is characterized by lack of lipids and apolipoprotein B [apoB] in plasma, fat malabsorption and various clinical manifestations. We describe a 12-month-old infant boy, born from consanguineous parents and presented with diarrhea, steatorrhea, growth retardation, hypothyroidism, intraventricu-lar brain cyst and kidney stones. The patient was diagnosed to have ABL and treated with dietary modification and oral fat-soluble vitamin replacement and followed until he reached 5 years of age
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Index:
IMEMR (Eastern Mediterranean)
Main subject:
Carrier Proteins
/
Infant
Type of study:
Case report
Limits:
Humans
/
Infant
/
Male
Language:
English
Journal:
Middle East J. Dig. Dis.
Year:
2015
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