European journal of pediatrics · 2003
Hair anomalies as a sign of mitochondrial disease.
СтатьяНазвание и аннотация: Перевод в очереди
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Silengo Margherita, Valenzise Mariella, Spada Marco, Ferrero Giovanni B, Ferraris Silvio, Dassi Patrizia, Jarre Laura
Аннотация
UNLABELLED: In 8 out of 25 children with a mitochondrial disorder, slow growing, sparse and fragile hair was observed as an early sign of their disease. Microscopic examination of the hair showed the presence of trichorrhexis nodosa and pili torti. Hair abnormalities can be added to the wide clinical spectrum of mitochondrial disorders.
CONCLUSION: Microscopic hair examination is an easy, first level diagnostic tool that can lead to a suspected mitochondrial defect in the early stages of the disease, before symptoms of progressive multi-organ involvement develop.
CONCLUSION: Microscopic hair examination is an easy, first level diagnostic tool that can lead to a suspected mitochondrial defect in the early stages of the disease, before symptoms of progressive multi-organ involvement develop.