Buscar
Mostrando ítems 1-10 de 159
Genotype and natural history in unrelated individual with phenylketonuria and autistic behavior
(Associa????o Arquivos de Neuro-Psiquiatria Dr. Oswaldo Lange, 2007-06)
Phenylketonuria, congenital hypothyroidism and haemoglobinopathies: public health issues for a Brazilian newborn screening programFenilcetonúria, hipotireoidismo congênito e hemoglobinopatias: questões de saúde pública para um programa de triagem neonatal brasileiro
(Escola Nacional de Saúde Pública Sérgio Arouca, 2018)
Genotype and natural history in unrelated individual with phenylketonuria and autistic behavior
(Associação Arquivos de Neuro-Psiquiatria Dr. Oswaldo Lange, 2007-06)
We describe three unrelated individuals, two males (ages 35 and 9) and a female (age 8) presenting with late diagnosed phenylketonuria (PKU) and autistic behavior, all showing poor adhesion to the dietary treatment resulting ...
Genotype and natural history in unrelated individuals with phenylketonuria and autistic behavior
(Assoc Arquivos De Neuro- PsiquiatriaSao Paulo SpBrasil, 2007)
New Parents' Guide to PKU.
(Universidad de Belgrano - Documentos CEEGMD - Centro para el estudio de enfermedades genéticas, metabólicas y discapacidades. Facultad de Ciencias Exactas, )
The purpose of this booklet is to help to familiarize you, as new parents of a
child with phenylketonuria (called PKU), with PKU and its treatment. It will
also help to orient you to the PKU clinic and the people there ...
A Babysitters' Guide to PKU.
(Universidad de Belgrano - Documentos CEEGMD - Centro para el estudio de enfermedades genéticas, metabólicas y discapacidades. Facultad de Ciencias Exactas -, 1987)
You are babysitting a child and there is a special restriction. The child has PKU and you
have never before heard of that.
PKU, stands for "phenylketonuria"
This child's body cannot use protein foods which contain ...
A Teacher's Guide to PKU
(Universidad de Belgrano - Documentos CEEGMD - Centro para el estudio de enfermedades genéticas, metabólicas y discapacidades. Facultad de Ciencias Exactas, 1985)
Phenylketonuria (or PKU) is an inherited disorder of protein metabolism. Children with PKU do not
have a functioning enzyme to metabolize or break down amino acid call phenylalanine (PHE for
short), which is found in ...
Phenylketonuria (PKU): Screening and Management
(Universidad de Belgrano - Documentos CEEGMD - Centro para el estudio de enfermedades genéticas, metabólicas y discapacidades. Facultad de Ciencias Exactas, 2000)
INTRODUCTION
Phenylketonuria or PKU is a rare, inherited metabolic disorder that, if untreated, causes mental retardation. Approximately
one of every 10,000 infants in the United States is born with PKU, which usually ...