Literature DB >> 20404749

Early diagnosis and treatment of cobalamin deficiency of infancy owing to occult maternal pernicious anemia.

Siddharth Banka1, Ruth Roberts, Dianne Plews, William G Newman.   

Abstract

SUMMARY: We report case of an infant who presented with failure to thrive and developmental delay at 4 months of age. He was diagnosed to have vitamin B12 deficiency and antibodies to intrinsic factor secondary to undiagnosed maternal pernicious anemia. The child was treated with hydroxocobalamin and now at 2 years of age, he is developing and growing within normal range. We review the literature on this rare cause of cobalamin deficiency in infants. We highlight the factors determining the outcome and situations where raised index of suspicion could help in recognizing this preventable cause of developmental delay and learning difficulties.

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Year:  2010        PMID: 20404749     DOI: 10.1097/MPH.0b013e3181d74719

Source DB:  PubMed          Journal:  J Pediatr Hematol Oncol        ISSN: 1077-4114            Impact factor:   1.289


  6 in total

1.  Severe megaloblastic anaemia in an infant.

Authors:  Vera Rodrigues; Alexandra Dias; Maria João Brito; Isabel Galvão; Gonçalo Cordeiro Ferreira
Journal:  BMJ Case Rep       Date:  2011-05-16

2.  Vitamin B12 deficiency with intrinsic factor antibodies in an infant with poor growth and developmental delay.

Authors:  Kathleen McNeil; Dhiman Chowdhury; Lynette Penney; Mohsin Rashid
Journal:  Paediatr Child Health       Date:  2014-02       Impact factor: 2.253

3.  Neuroregression as an initial manifestation in a toddler with acquired pernicious anaemia.

Authors:  Sangeetha Yoganathan; Maya Mary Thomas; Sarah Mathai; Urmi Ghosh
Journal:  BMJ Case Rep       Date:  2015-12-17

4.  Vitamin composition of ethnic foods commonly consumed in Europe.

Authors:  Santosh Khokhar; Olusegun James Oyelade; Luisa Marletta; Danit Shahar; Jane Ireland; Stefaan de Henauw
Journal:  Food Nutr Res       Date:  2012-04-02       Impact factor: 3.894

Review 5.  Vitamin B12 deficiency: case report and review of literature.

Authors:  Brahim El Hasbaoui; Nadia Mebrouk; Salahiddine Saghir; Abdelhkim El Yajouri; Rachid Abilkassem; Aomar Agadr
Journal:  Pan Afr Med J       Date:  2021-03-04

6.  Profound vitamin D deficiency in four siblings with Imerslund-Grasbeck syndrome with homozygous CUBN mutation.

Authors:  Jose I R Ciancio; Mark Furman; Siddharth Banka; Stephanie Grunewald
Journal:  JIMD Rep       Date:  2019-07-26
  6 in total

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