Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 1 de 1
Filtrar
Mais filtros










Base de dados
Tipo de estudo
Intervalo de ano de publicação
1.
J Inherit Metab Dis ; 25(1): 35-40, 2002 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-11999978

RESUMO

We describe a patient diagnosed with lethal perinatal hypophosphatasia with a unique clinical presentation of convulsions that responded to vitamin B6. Genomic DNA sequence analysis of the tissue-nonspecific alkaline phosphatase (TNSALP) gene revealed two missense mutations: a G-to-A transition resulting in a Glu to Lys at codon 274 (E274K), and a G-to-C transversion resulting in a Gly to Arg at codon 309 (G309R). The first mutation was maternally transmitted and was previously characterized as a moderate one, whereas the latter was paternally transmitted and has not been previously reported. Phenotype/genotype correlation indicates that G309R is a deleterious mutation that can lead to seizures and a lethal outcome, as was demonstrated in our patient.


Assuntos
Fosfatase Alcalina/genética , Hipofosfatasia/enzimologia , Mutação de Sentido Incorreto , Convulsões/enzimologia , Arginina/genética , Feminino , Ácido Glutâmico/genética , Humanos , Hipofosfatasia/complicações , Hipofosfatasia/genética , Recém-Nascido , Lisina/genética , Convulsões/complicações , Convulsões/genética
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...