1.
Revue Marocaine des Maladies de l'Enfant. 2005; (5): 76-77
en Francés
| IMEMR
| ID: emr-74522
Asunto(s)
Humanos , Masculino , Diagnóstico Prenatal , Tirosinemias/etiología , Anomalías Congénitas
2.
Revue Marocaine des Maladies de l'Enfant. 2005; (6): 68-69
en Francés
| IMEMR
| ID: emr-74539
3.
Revue Marocaine des Maladies de l'Enfant. 2005; (6): 69-70
en Francés
| IMEMR
| ID: emr-74540
Asunto(s)
Humanos , Masculino , Ceruloplasmina , Cobre , Síndrome del Pelo Ensortijado/terapia , Lactante
4.
Revue Marocaine des Maladies de L'Enfant. 2005; (7): 49-50
en Francés
| IMEMR
| ID: emr-74557
5.
Maghreb Medical. 2003; 23 (365): 42-4
en Francés
| IMEMR
| ID: emr-63350
6.
Revue Maghrebine de Pediatrie [La]. 2000; 10 (5): 249-53
en Francés
| IMEMR
| ID: emr-55171
Asunto(s)
Humanos , Masculino , Femenino , Enfermedades Inflamatorias del Intestino/terapia , Enfermedad de Crohn , Colitis Ulcerosa , Colitis , Niño
7.
Maroc Medical. 1997; 19 (2): 21-26
en Francés
| IMEMR
| ID: emr-45500
RESUMEN
We report one case primary hyperoxaluria in a fourteen year old child. The diagnosis was possible after the discovery of oxalate of Ca crystals in kidneys and marrow. Our case illustrates some of the clinical and paraclinical characteristics of oxalosis. It also proves how severe the kidney failure could be in this disease. The diagnosis criteria and the therapeutic possibilities that lead to improve this diseasee are also discussed here