Child Neurology: Hereditary Folate Malabsorption

Author:

Huddar Akshata,Chiplunkar Shwetha,Nagappa Madhu,Govindaraj PeriyasamyORCID,Sinha Sanjib,Taly Arun B.,Sankaran Bindu ParayilORCID

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Reference10 articles.

1. Kronn D , Goldman ID . Hereditary folate malabsorption: 2008 June 17 (updated 2017 April 27). In: Adam MP , Ardinger HH , Pagon RA , et al , eds. GeneReviews®. University of Washington; 1993–2020.

2. The proton-coupled folate transporter (PCFT-SLC46A1) and the syndrome of systemic and cerebral folate deficiency of infancy: Hereditary folate malabsorption

3. Hereditary folate malabsorption with extensive intracranial calcification;Ahmad;Indian Pediatr.,2015

4. Infantile tremor syndrome: a review and critical appraisal of its etiology;Goraya;J Pediatr Neurosci.,2016

5. Relapsing megaloblastic anemia in an infant due to a specific defect in gastrointestinal absorption of folic acid;Lubhy;Am J Dis Child.,1961

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