Congenital ocular motor apraxia associated with myopathy, external hydrocephalus and NADH dehydrogenase deficiency

Brain and Development

Volumn 20, Issue 3, 1998, Pages 175-178

  Puñal, Jesús Eirís ^a   Rodríguez, Eladio ^a   Pintos, Elena ^b   Campos, Yolanda ^c   Castro Gago, Manuel ^a  

^a Serv Neuropediatria Hosp Gen G   (Spain)

^b HOSPITAL CLÍNICO UNIVERSITARIO   (Spain)

^c HOSPITAL UNIVERSITARIO 12 DE OCTUBRE   (Spain)

Author keywords

Congenital ocular motor apraxia; Mitochondrial dysfunction; NADH dehydrogenase deficiency

Indexed keywords

LACTIC ACID; PYRUVIC ACID; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE;

APRAXIA; ARTICLE; CASE REPORT; ENZYME DEFICIENCY; EYE MOVEMENT; EYE MOVEMENT DISORDER; FEMALE; HEAD MOVEMENT; HUMAN; HYDROCEPHALUS; INFANT; LACTATE BLOOD LEVEL; MITOCHONDRIAL MYOPATHY; MYOPATHY; PSYCHOMOTOR RETARDATION;

APRAXIAS; FEMALE; HUMANS; HYDROCEPHALUS; INFANT; MITOCHONDRIA, MUSCLE; MUSCULAR DISEASES; NADH DEHYDROGENASE; OCULOMOTOR MUSCLES; TOMOGRAPHY, X-RAY COMPUTED;

EID: 0344193637     PISSN: 03877604     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0387-7604(98)00009-6     Document Type: Article

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