Delayed Diagnosis of Congenital Hypothyroidism in a Child with Trisomy 21 and Biotinidase Deficiency and Successful Use of Levothyroxine Sodium Oral Solution

Endocrine disorders are more common and appear earlier in people with trisomy 21 (T21) than in the general population, with thyroid dysfunction being the most common, including both congenital and acquired hypothyroidism. The treatment for biotinidase deficiency, a condition that occurs in approxima...

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Detalles Bibliográficos
Autor principal: Feldt, Matthew M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7773459/
https://www.ncbi.nlm.nih.gov/pubmed/33425403
http://dx.doi.org/10.1155/2020/8883969

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7773459/
https://www.ncbi.nlm.nih.gov/pubmed/33425403
http://dx.doi.org/10.1155/2020/8883969

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