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Perinatal hypophosphatasia presenting as neonatal epileptic encephalopathy with abnormal neurotransmitter metabolism secondary to reduced co-factor pyridoxal-5'-phosphate availability.
Balasubramaniam, Shanti; Bowling, Frank; Carpenter, Kevin; Earl, John; Chaitow, Jeffrey; Pitt, James; Mornet, Etienne; Sillence, David; Ellaway, Carolyn.
Afiliação
  • Balasubramaniam S; Genetic Metabolic Disorders Service, The Children's Hospital at Westmead, Sydney, Australia.
J Inherit Metab Dis ; 33 Suppl 3: S25-33, 2010 Dec.
Article em En | MEDLINE | ID: mdl-20049532
We describe two neonates presenting with perinatal hypophosphatasia and severe epileptic encephalopathy resulting in death. Both had increased levels of urinary vanillactate, indicating functional deficiency of aromatic amino acid decarboxylase, a pyridoxal-5-phosphate (PLP)-dependent enzyme required for dopamine and serotonin biosynthesis. Clinical findings and results of subsequent metabolic investigations were consistent with secondary pyridoxine-deficient encephalopathy. These patients highlight the importance of tissue non-specific alkaline phosphatase in the neuronal PLP-dependent metabolism of neurotransmitters. In addition, the disturbance of PLP metabolism appears to underlie the predominant neurological presentation in our patients. We recommend the measurement of serum alkaline phosphatase (ALP) during the assessment of perinatal seizures.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fosfato de Piridoxal / Piridoxaminafosfato Oxidase / Deficiência de Vitamina B 6 / Convulsões / Encefalopatias Metabólicas / Monoaminas Biogênicas / Hipóxia-Isquemia Encefálica / Fosfatase Alcalina / Hipofosfatasia / Mutação Tipo de estudo: Diagnostic_studies Limite: Female / Humans / Male / Newborn Idioma: En Revista: J Inherit Metab Dis Ano de publicação: 2010 Tipo de documento: Article País de afiliação: Austrália

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fosfato de Piridoxal / Piridoxaminafosfato Oxidase / Deficiência de Vitamina B 6 / Convulsões / Encefalopatias Metabólicas / Monoaminas Biogênicas / Hipóxia-Isquemia Encefálica / Fosfatase Alcalina / Hipofosfatasia / Mutação Tipo de estudo: Diagnostic_studies Limite: Female / Humans / Male / Newborn Idioma: En Revista: J Inherit Metab Dis Ano de publicação: 2010 Tipo de documento: Article País de afiliação: Austrália