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Tyrosinemia type III: a case report of siblings and literature review ; Tirosinemia tipo III: descrição de caso clínico em irmãos e revisão da literatura

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  • معلومة اضافية
    • بيانات النشر:
      Zeppelini Publishers/ Sociedade de Pediatria de São Paulo
    • الموضوع:
      2021
    • Collection:
      National Health Institute, Portugal: Repositório Científico
    • نبذة مختصرة :
      in English, Portuguese ; Objective: Tyrosinemia type III (HT III) is the rarest form of tyrosinemia, and the full clinical spectrum of this disorder is still unknown. The neurological involvement varies, including intellectual impairment and attention deficit disorder with hyperactivity (ADHD). We report the case of two siblings diagnosed with HT III at different ages. Case description: The index case was diagnosed by newborn screening for endocrine and metabolic disorders, starting a low-protein diet immediately, with a consistent decrease in tyrosine levels. By the age of three, the child displayed a hyperactive behavior, starting treatment for ADHD two years later. At seven years of age, he shows a slight improvement in terms of behavior and attention span and has a cognitive performance slightly lower than his peers, despite maintaining acceptable tyrosine levels. His sister, who had a history of ADHD since age five, was diagnosed with HT III after family screening at the age of eight. Despite initiating a dietetic treatment, her behavior did not improve, and she has a mild intellectual impairment. Comments: This is the first case report describing siblings with HT III who underwent nutritional treatment with a low-protein diet in different phases of life, with a better neurological and behavioral evaluation in the patient who started treatment earlier. ; Objetivo: A tirosinemia tipo III (TT III) é a forma mais rara das tirosinemias e o espectro clínico desta entidade não está totalmente esclarecido. O envolvimento neurológico é variável, incluindo o atraso cognitivo ou transtorno do déficit de atenção com hiperatividade (TDAH). Descrevemos o caso de dois irmãos que foram diagnosticados com TT III em idades diferentes. Descrição dos casos: O caso índice foi diagnosticado no contexto do rastreio endócrino-metabólico neonatal, tendo iniciado imediatamente dieta hipoproteica, com redução consistente dos níveis de tirosina. Por volta dos três anos, foi detectado um comportamento hiperativo, tendo ...
    • ISSN:
      0103-0582
    • Relation:
      https://www.scielo.br/scielo.php?script=sci_arttext&pid=S0103-05822020000100610&tlng=en; Rev Paul Pediatr. 2020 Jun 5;38:e2018158. Epub 2020 May 22. doi:10.1590/1984-0462/2020/38/2018158. eCollection 2020.; http://hdl.handle.net/10400.18/7660
    • الرقم المعرف:
      10.1590/1984-0462/2020/38/2018158
    • Rights:
      openAccess ; http://creativecommons.org/licenses/by/4.0/
    • الرقم المعرف:
      edsbas.A85B1C33