The Enigma of Periorificial Desquamating Lesions in a Child

Biotinidase deficiency (BD) is a rare autosomal recessive, vitamin-responsive inborn error of metabolism associated with a wide spectrum of dermatological, neurological, auditory, and metabolic abnormalities. This case report reiterates that a high index of suspicion in childhood diseases with perio...

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Detalles Bibliográficos
Autores principales: Choudhary, Ankita, Pandya, Rutvi M., Joshi, Rima, Shah, Bela J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10115314/
https://www.ncbi.nlm.nih.gov/pubmed/37089844
http://dx.doi.org/10.4103/idoj.idoj_322_22

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10115314/
https://www.ncbi.nlm.nih.gov/pubmed/37089844
http://dx.doi.org/10.4103/idoj.idoj_322_22

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