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Coexistence of type 1 diabetes mellitus and spinal muscular atrophy in an 8-year-old girl: a case report.
Borkowska, Anna; Jankowska, Agnieszka; Szlagatys-Sidorkiewicz, Agnieszka; Sztangierska, Beata; Liberek, Anna; Plata-Nazar, Katarzyna; Kaminska, Barbara.
Afiliação
  • Borkowska A; Department of Pediatrics, Pediatric Gastroenterology, Hepatology and Nutrition.
  • Jankowska A; Department of Pediatrics, Pediatric Gastroenterology, Hepatology and Nutrition.
  • Szlagatys-Sidorkiewicz A; Department of Pediatrics, Pediatric Gastroenterology, Hepatology and Nutrition.
  • Sztangierska B; Department of Pediatrics, Hematology, Oncology and Endocrinology.
  • Liberek A; Faculty of Health Sciences with Subfaculty of Nursing, Medical University of Gdansk, Gdansk, Poland.
  • Plata-Nazar K; Department of Pediatrics, Pediatric Gastroenterology, Hepatology and Nutrition.
  • Kaminska B; Department of Pediatrics, Pediatric Gastroenterology, Hepatology and Nutrition.
Acta Biochim Pol ; 62(1): 167-8, 2015.
Article em En | MEDLINE | ID: mdl-25669159
ABSTRACT
The spinal muscular atrophy is a rare autosomal recessive genetic disease characterized by the progressive loss of muscular strength. In its natural course the disease leads to death. Diabetes mellitus type 1 is an autoimmune metabolic disorder characterized by the disturbed insulin synthesis. This is a case report of an 8-year-old girl suffering from Werdnig Hoffman disease in whom DM1 was diagnosed. The unspecific clinical manifestation and diagnostic difficulties are presented in this paper. To the authors' knowledge, this is the first publication concerning the co-existence of these two medical conditions.
Assuntos
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Base de dados: MEDLINE Assunto principal: Atrofia Muscular Espinal / Diabetes Mellitus Tipo 2 Idioma: En Ano de publicação: 2015 Tipo de documento: Article
Buscar no Google
Base de dados: MEDLINE Assunto principal: Atrofia Muscular Espinal / Diabetes Mellitus Tipo 2 Idioma: En Ano de publicação: 2015 Tipo de documento: Article