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Biotinidase Deficiency Presenting as Recurrent Laryngeal Stridor

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References

  1. Strovel ET, Cowan TM, Scott AI, Wolf B. Laboratory diagnosis of biotinidase deficiency, 2017 update: a technical standard and guideline of the American College of Medical Genetics and Genomics. Genet Med. 2017;19(10).

  2. Venkataraman V, Balaji P, Panigrahi D, Jamal R. Biotinidase deficiency in childhood. Neurol India. 2013;61:411–3.

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  3. Baumgartner ER, Suormala TM, Wick H, et al. Biotidinase deficiency: a cause of subacute necrotizing encephalopathy (Leigh syndrome). Pediatr Res. 1989;26:260–6.

  4. Singh A, Lomash A, Pandey S, Kapoor S. Clinical, biochemical and outcome profile of biotinidase deficient patients from tertiary centre in northern India. J Clin Diagn Res. 2015;9(12):SC08–10.

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Authors and Affiliations

  1. Department of Pediatrics, Masonic Medical Centre for Children, Coimbatore, Tamil Nadu, India

    Sruthi Alanghat, Vidhya Marimuthu & M Ramaswamy

  2. Department of Gastroenterology, Masonic Medical Centre for Children, Coimbatore, Tamil Nadu, India

    John Matthai

  3. Department of Neurology, Masonic Medical Centre for Children, Coimbatore, Tamil Nadu, India

    R Manivasakan

Authors
  1. Sruthi Alanghat
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  2. John Matthai
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  3. Vidhya Marimuthu
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  4. R Manivasakan
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  5. M Ramaswamy
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Correspondence to Sruthi Alanghat.

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Alanghat, S., Matthai, J., Marimuthu, V. et al. Biotinidase Deficiency Presenting as Recurrent Laryngeal Stridor. Indian J Pediatr 88, 617–618 (2021). https://doi.org/10.1007/s12098-020-03635-y

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  • DOI: https://doi.org/10.1007/s12098-020-03635-y

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