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Non-ketotic hyperglycinaemia: a frequent, but poorly diagnosed and managed genetic disorder in Tunisia.
Nasrallah, Fahmi; Ben Chehida, Amel; Kraoua, Ichraf; Hadj-Taieb, Sameh; Sanhaji, Haifa; Tebib, Neji; Feki, Moncef; Kaabachi, Naziha.
Affiliation
  • Nasrallah F; University of Tunis El Manar, Faculty of Medicine of Tunis, Tunis, Tunisia fehmi56@yahoo.fr.
  • Ben Chehida A; Laboratory of Biochemistry, LR99ES11, Rabta Hospital, Tunis, Tunisia.
  • Kraoua I; Service of Pediatrics, LR12SP02, Rabta Hospital, Tunis, Tunisia.
  • Hadj-Taieb S; University of Tunis El Manar, Faculty of Medicine of Tunis, Tunis, Tunisia.
  • Sanhaji H; Service of Pediatrics, LR12SP02, Rabta Hospital, Tunis, Tunisia.
  • Tebib N; University of Tunis El Manar, Faculty of Medicine of Tunis, Tunis, Tunisia.
  • Feki M; Service of Child Neurology, LR18SP04, National Institute Mongi Ben Hmida of Neuroloy, Tunis, Tunisia.
  • Kaabachi N; University of Tunis El Manar, Faculty of Medicine of Tunis, Tunis, Tunisia.
Arch Dis Child ; 106(3): 311, 2021 03.
Article in En | MEDLINE | ID: mdl-32404439

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hyperglycinemia, Nonketotic / Glycine Type of study: Diagnostic_studies / Incidence_studies / Prognostic_studies Limits: Humans Country/Region as subject: Africa Language: En Journal: Arch Dis Child Year: 2021 Document type: Article Affiliation country: Túnez

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hyperglycinemia, Nonketotic / Glycine Type of study: Diagnostic_studies / Incidence_studies / Prognostic_studies Limits: Humans Country/Region as subject: Africa Language: En Journal: Arch Dis Child Year: 2021 Document type: Article Affiliation country: Túnez