| Literature DB >> 30333199 |
Nell Freeman-Romilly1, Leena Mewasingh2, Annette Coomer2, Caroline Foster2.
Abstract
An 18-year-old black African man with well-controlled perinatally acquired HIV-1 was diagnosed in late adolescence with the unrelated diagnoses of Charcot-Marie-Tooth type 1A (CMT1A), epilepsy due to polymicrogyria and subsequently developed severe depression. The CMT1A diagnosis occurred after transfer of care from a local paediatric HIV service to a tertiary paediatric referral centre and was precipitated by recognition of a history and neurological signs not typically associated with perinatal HIV. The case resulted in the establishment of a quarterly combined paediatric HIV and paediatric neurology multidisciplinary team clinic to assess children and adolescents living with HIV with neurological symptoms. © BMJ Publishing Group Limited 2018. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: Hiv / Aids; child and adolescent psychiatry (paediatrics); neurology; neuromuscular disease; peripheral nerve disease
Mesh:
Year: 2018 PMID: 30333199 PMCID: PMC6202967 DOI: 10.1136/bcr-2018-226042
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X