Hair and skin disorders as signs of mitochondrial disease

Pediatrics

Volumn 103, Issue 2, 1999, Pages 428-433

  Bodemer, Christine ^a,e   Rötig, Agnès ^b   Rustin, Pierre ^b   Cormier, Valerie ^b   Niaudet, Patrick ^c   Saudubray, Jean Marie ^d   Rabier, Denis ^e   Munnich, Arnold ^b   Yves, De Prost ^a  

^a Service de Dermatologie   (France)

^b INSERM   (France)

^c Serv de Néphrologie Pediat   (France)

^d Dept Maladies Metaboliques G ^*  (France)

^e HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

Alopecia; Mitochondrial disease; Pigmentation disorders; Trichothiodystrophy

Indexed keywords

ACROCYANOSIS; ALOPECIA; ARTICLE; CELL CULTURE; CHILD; COHORT ANALYSIS; DIAGNOSTIC ACCURACY; DISORDERS OF MITOCHONDRIAL FUNCTIONS; EARLY DIAGNOSIS; FEMALE; HAIR DISEASE; HUMAN; HYPERTRICHOSIS; MAJOR CLINICAL STUDY; MALE; MASS SCREENING; OXIDATIVE PHOSPHORYLATION; PIGMENT DISORDER; PRIORITY JOURNAL; SKIN DISEASE; SYMPTOMATOLOGY;

EID: 0344731064     PISSN: 00314005     EISSN: None     Source Type: Journal    
DOI: 10.1542/peds.103.2.428     Document Type: Article

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