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Mialgias post ejercicios como forma de presentación de una distrofinopatía / Post exercise myalgias as form of dystrophynopathy
Kleinsteuber S., Karin; Rocco P., Paola; Herrera C., Luisa; Vainzof, Mariz; Birke L., María Eliana; Yáñez Z., Manuel; Flandes J., Ana; Zatz, Mayana; Carvallo de Saint Quentin, Pilar; Avaria Benapres, María de los Angeles.
Affiliation
  • Kleinsteuber S., Karin; Hospital Clínico San Borja Arriarán. Servicio de Neuropsiquiatría Infantil.
  • Rocco P., Paola; Hospital Clínico San Borja Arriarán. Servicio de Neuropsiquiatría Infantil.
  • Herrera C., Luisa; Hospital Clínico San Borja Arriarán. Servicio de Neuropsiquiatría Infantil.
  • Vainzof, Mariz; Hospital Clínico San Borja Arriarán. Servicio de Neuropsiquiatría Infantil.
  • Birke L., María Eliana; Hospital Clínico San Borja Arriarán. Servicio de Neuropsiquiatría Infantil.
  • Yáñez Z., Manuel; Hospital Clínico San Borja Arriarán. Servicio de Neuropsiquiatría Infantil.
  • Flandes J., Ana; Hospital Clínico San Borja Arriarán. Servicio de Neuropsiquiatría Infantil.
  • Zatz, Mayana; Hospital Clínico San Borja Arriarán. Servicio de Neuropsiquiatría Infantil.
  • Carvallo de Saint Quentin, Pilar; Hospital Clínico San Borja Arriarán. Servicio de Neuropsiquiatría Infantil.
  • Avaria Benapres, María de los Angeles; Hospital Clínico San Borja Arriarán. Servicio de Neuropsiquiatría Infantil.
Rev. méd. Chile ; 128(7): 772-7, jul. 2000. ilus
Article in Spanish | LILACS | ID: lil-270888
Responsible library: CL1.1
RESUMO
Cramps and myalgias are frequent presentations of many disorders whose diagnosis is generally difficult. Among the unusual causes stand the milder phenotypes of dystrophinopathies, which are caused, just as Duchenne and BeckerÕs dystrophy, by mutations in the dystrophin gene. An 8 year-old boy presented severe muscle pain on exercise and serum rise in creatine kinase over 1000 U/l. He had normal muscle power and mild calf hypertrophy. The molecular analysis by polymerase chain reaction (PCR) of the dystrophin gene showed deletions of exons 45 to 51. Dystrophin analysis by Western blot revealed a dystrophin of reduced quantity and molecular weight. Emphasis is made to include dystrophinopathies in the differential diagnosis of myalgias and the usefulness of molecular genetic techniques in the identification of these disorders
Subject(s)
Full text: Available Collection: International databases Database: LILACS Main subject: Immunohistochemistry / Dystrophin / Muscular Dystrophies Type of study: Diagnostic study / Prognostic study Limits: Child / Humans / Male Language: Spanish Journal: Rev. méd. Chile Journal subject: Medicine Year: 2000 Document type: Article / Project document
Full text: Available Collection: International databases Database: LILACS Main subject: Immunohistochemistry / Dystrophin / Muscular Dystrophies Type of study: Diagnostic study / Prognostic study Limits: Child / Humans / Male Language: Spanish Journal: Rev. méd. Chile Journal subject: Medicine Year: 2000 Document type: Article / Project document
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