Literature DB >> 25638192

Hereditary folate malabsorption with extensive intracranial calcification.

Ikhlas Ahmad1, Gousia Mukhtar, Javed Iqbal, Syed Wajid Ali.   

Abstract

BACKGROUND: Anemia is a common accompaniment of cerebral palsy, mental retardation and neurodegenerative disorders. CLINICAL CHARACTERISTICS: A 4-year-old boy with chronic megaloblastic anemia, global developmental delay, seizures, intracranial calcification and new onset neuro-regression. OBSERVATION: A diagnosis of hereditary folate malabsorption was made, and he was put on oral and injectable folinic acid. OUTCOME: Marked improvement at 6 month follow up. MESSAGE: Hereditary folate malabsorption should be suspected in any child having megaloblastic anemia and neuro degeneration disorder.

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Mesh:

Year:  2015        PMID: 25638192     DOI: 10.1007/s13312-015-0571-8

Source DB:  PubMed          Journal:  Indian Pediatr        ISSN: 0019-6061            Impact factor:   1.411


  3 in total

1.  Role of Intramuscular Levofolinate Administration in the Treatment of Hereditary Folate Malabsorption: Report of Three Cases.

Authors:  Emanuela Manea; Paul Gissen; Simon Pope; Simon J Heales; Spyros Batzios
Journal:  JIMD Rep       Date:  2017-07-07

2.  Hereditary Folate Malabsorption presenting as neutropenic fever in a newborn from the first Palestinian family with the novel SLC46A1-mutation, A-case-report.

Authors:  Fajr M A Sarhan; Afnan W M Jobran; Islam I A Mansour; Osama N Dukmak; Mohammed A M Rashed; Dina M A Hamdan; Israa A A Abdalhadi
Journal:  Ann Med Surg (Lond)       Date:  2022-07-31

3.  Hereditary folate malabsorption with a novel mutation on SLC46A1: A case report.

Authors:  Jianmin Tan; Xiujuan Li; Yi Guo; Lingling Xie; Juan Wang; Jiannan Ma; Li Jiang
Journal:  Medicine (Baltimore)       Date:  2017-12       Impact factor: 1.817

  3 in total

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