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Atypical onset of nephropathic infantile cystinosis in a Russian patient with rare CTNS mutation.
Anastasiya, Kozina A; Elena, Okuneva G; Natalia, Baryshnikova V; Anna, Krasnenko Yu; Kirill, Tsukanov Yu; Olesya, Klimchuk I; Tatiana, Nikishina A; Inessa, Fedoniuk D; Ekaterina, Surkova I; Peter, Shatalov A; Valery, Ilinsky V.
Afiliação
  • Anastasiya KA; Institute of Biomedical Chemistry Moscow Russia.
  • Elena OG; Genotek Ltd. Moscow Russia.
  • Natalia BV; Genotek Ltd. Moscow Russia.
  • Anna KY; Genotek Ltd. Moscow Russia.
  • Kirill TY; Pirogov Russian National Research Medical University Moscow Russia.
  • Olesya KI; Genotek Ltd. Moscow Russia.
  • Tatiana NA; Genotek Ltd. Moscow Russia.
  • Inessa FD; Genotek Ltd. Moscow Russia.
  • Ekaterina SI; Veltischev Research and Clinical Institute for Pediatrics of the Pirogov Russian National Research Medical University Moscow Russia.
  • Peter SA; Russian Children's Clinical Hospital Moscow Russia.
  • Valery IV; Genotek Ltd. Moscow Russia.
Clin Case Rep ; 6(9): 1871-1876, 2018 Sep.
Article em En | MEDLINE | ID: mdl-30214781
We report a Russian patient with atypical onset of infantile nephropathic cystinosis. The disease debuted with vomiting and loss of weight and motor skills. Nephropathic changes appeared 6 months after onset of disease. Exome sequencing can be useful for diagnosing cystinosis in patients with neurological abnormalities before onset of nephropathic symptoms.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article