The 20 Best Primary Carnitine Deficiency Doctors in Brazil
Find the Top Primary Carnitine Deficiency Experts and Specialists
Jessica Faverzani practices practicing medicine in Porto Alegre, Brazil. Ms. Faverzani is rated as an Advanced expert by MediFind in the treatment of Primary Carnitine Deficiency. She is also highly rated in 5 other conditions, according to our data. Her clinical expertise encompasses Phenylketonuria (PKU), Glutaric Acidemia Type 1, Maple Syrup Urine Disease, and Orotic Aciduria Type 1.
Franciele Lopes practices practicing medicine in Porto Alegre, Brazil. Lopes is rated as an Experienced expert by MediFind in the treatment of Primary Carnitine Deficiency. They are also highly rated in 6 other conditions, according to our data. Their clinical expertise encompasses Carbamoyl Phosphate Synthetase 1 Deficiency, Argininosuccinic Aciduria, Orotic Aciduria Type 1, and Urea Cycle Disorders (UCD).
Angela Sitta practices practicing medicine in Porto Alegre, Brazil. Ms. Sitta is rated as an Experienced expert by MediFind in the treatment of Primary Carnitine Deficiency. She is also highly rated in 6 other conditions, according to our data. Her clinical expertise encompasses Glutaric Acidemia Type 1, Maple Syrup Urine Disease, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, and Phenylketonuria (PKU).
Tatiane Hammerschmidt practices practicing medicine in Porto Alegre, Brazil. Hammerschmidt is rated as an Experienced expert by MediFind in the treatment of Primary Carnitine Deficiency. They are also highly rated in 4 other conditions, according to our data. Their clinical expertise encompasses Niemann-Pick Disease, Non-Langerhans-Cell Histiocytosis, Histiocytosis, and Reticulohistiocytoma.
Moacir Wajner practices practicing medicine in Porto Alegre, Brazil. Wajner is rated as an Experienced expert by MediFind in the treatment of Primary Carnitine Deficiency. They are also highly rated in 25 other conditions, according to our data. Their clinical expertise encompasses Medium-Chain Acyl-CoA Dehydrogenase Deficiency, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, Glutaric Acidemia Type 1, and Sulfite Oxidase Deficiency.
Daniella De Moura Coelho practices practicing medicine in Porto Alegre, Brazil. Ms. De Moura Coelho is rated as an Experienced expert by MediFind in the treatment of Primary Carnitine Deficiency. She is also highly rated in 5 other conditions, according to our data. Her clinical expertise encompasses 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, Maple Syrup Urine Disease, Orotic Aciduria Type 1, and Glutaric Acidemia Type 1.
Caroline Mescka practices practicing medicine in Porto Alegre, Brazil. Ms. Mescka is rated as an Experienced expert by MediFind in the treatment of Primary Carnitine Deficiency. She is also highly rated in 1 other condition, according to our data. Her clinical expertise encompasses Maple Syrup Urine Disease, Phenylketonuria (PKU), Infant Hyperglycemia, and Primary Carnitine Deficiency.
Marion Deon practices practicing medicine in Porto Alegre, Brazil. Deon is rated as an Experienced expert by MediFind in the treatment of Primary Carnitine Deficiency. They are also highly rated in 4 other conditions, according to our data. Their clinical expertise encompasses Adrenoleukodystrophy (ALD), Phenylketonuria (PKU), Medium-Chain Acyl-CoA Dehydrogenase Deficiency, and Addison's Disease.
Gilian Guerreiro practices practicing medicine in Porto Alegre, Brazil. Ms. Guerreiro is rated as an Experienced expert by MediFind in the treatment of Primary Carnitine Deficiency. She is also highly rated in 2 other conditions, according to our data. Her clinical expertise encompasses Glutaric Acidemia Type 1, Maple Syrup Urine Disease, Phenylketonuria (PKU), and Primary Carnitine Deficiency.
Carmen Vargas practices practicing medicine in Porto Alegre, Brazil. Ms. Vargas is rated as an Experienced expert by MediFind in the treatment of Primary Carnitine Deficiency. She is also highly rated in 20 other conditions, according to our data. Her clinical expertise encompasses Maple Syrup Urine Disease, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, Glutaric Acidemia Type 1, and Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome).
Last Updated: 06/30/2026