Literature DB >> 6543837

Familial hypobetalipoproteinaemia.

E Roma, D Klontza, M Kairis, A Pangalis, J Karpouzas, N Matsaniotis.   

Abstract

Familial hypobetalipoproteinaemia is a rare condition and is usually asymptomatic in heterozygotes. We report a case of hypobetalipoproteinaemia in an 8-month-old boy presenting with diarrhoea and failure to thrive since birth, who has been successfully treated with dietary restriction and large oral doses of vitamin E. This disease is one of the causes of chronic diarrhoea in childhood and its early treatment probably prevents irreversible retinal and nervous system lesions in later life.

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Year:  1984        PMID: 6543837

Source DB:  PubMed          Journal:  Helv Paediatr Acta        ISSN: 0018-022X


  4 in total

1.  Unusual presentation of three siblings with familial heterozygous hypobetalipoproteinaemia.

Authors:  V Kairamkonda; M Dalzell
Journal:  Eur J Pediatr       Date:  2003-01-11       Impact factor: 3.183

2.  Homozygous hypobetalipoproteinaemia and phenylketonuria.

Authors:  J U Leititis; M Stahl; W Tackmann; H Wick; A Wildberg
Journal:  Eur J Pediatr       Date:  1985-07       Impact factor: 3.183

Review 3.  Breast cancer resistance mechanisms: challenges to immunotherapy.

Authors:  Ann Hanna; Justin M Balko
Journal:  Breast Cancer Res Treat       Date:  2021-07-28       Impact factor: 4.872

Review 4.  Dosage and formulation issues: oral vitamin E therapy in children.

Authors:  Tone Westergren; Betty Kalikstad
Journal:  Eur J Clin Pharmacol       Date:  2009-10-13       Impact factor: 2.953

  4 in total

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