Phenylketonuria in three siblings
Pract Neurol
.
2023 Nov 23;23(6):525-526.
doi: 10.1136/pn-2023-003815.
Authors
Igor de Assis Franco
1
,
Ane Maria Dos Anjos Florinda
2
,
Fabrício Guimarães Gonçalves
3
,
Marcelo Masruha Rodrigues
4
,
Thiago Cardoso Vale
5
Affiliations
1
Department of Neurology, Hospital e Maternidade São José, Conselheiro Lafaiete, Brazil igorafranco1@gmail.com.
2
Department of Neurology, Hospital e Maternidade São José, Conselheiro Lafaiete, Brazil.
3
Department of Neuroradiology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
4
Department of Neurology and Neurosurgery, Universidade Federal de São Paulo, Sao Paulo, Brazil.
5
Neurology, Universidade Federal de Juiz de Fora, Juiz de Fora, Brazil.
PMID:
37487703
DOI:
10.1136/pn-2023-003815
No abstract available
Keywords:
epilepsy; genetics; mental retardation; metabolic disease.
MeSH terms
Humans
Phenylketonurias* / complications
Phenylketonurias* / diagnosis
Phenylketonurias* / genetics
Siblings*