The 20 Best Dihydrolipoamide Dehydrogenase Deficiency Doctors Near Me in Ankara, TR
Find the Top Dihydrolipoamide Dehydrogenase Deficiency Experts and Specialists
Mustafa Kılıc practices practicing medicine in Ankara, Turkey. Mr. Kılıc is rated as an Experienced expert by MediFind in the treatment of Dihydrolipoamide Dehydrogenase Deficiency. He is also highly rated in 6 other conditions, according to our data. His clinical expertise encompasses Fucosidosis, Visceromegaly, Glycine Encephalopathy, and Hypotonia.
Abdullatif Bakır practices practicing medicine in Ankara, Turkey. Mr. Bakır is rated as an Experienced expert by MediFind in the treatment of Dihydrolipoamide Dehydrogenase Deficiency. He is also highly rated in 2 other conditions, according to our data. His clinical expertise encompasses Chromosome 3q Duplication, Cone Rod Dystrophy Amelogenesis Imperfecta, Renal Tubular Acidosis, and Jalili Syndrome.
Serdar Ceylaner practices practicing medicine in Ankara, Turkey. Mr. Ceylaner is rated as an Experienced expert by MediFind in the treatment of Dihydrolipoamide Dehydrogenase Deficiency. He is also highly rated in 52 other conditions, according to our data. His clinical expertise encompasses Hypotonia, Glucose-Galactose Malabsorption Deficiency, Camptodactyly Syndrome Guadalajara Type 2, Hormone Replacement Therapy (HRT), and Craniectomy.
Abdullah Sezer practices practicing medicine in Ankara, Turkey. Mr. Sezer is rated as an Experienced expert by MediFind in the treatment of Dihydrolipoamide Dehydrogenase Deficiency. He is also highly rated in 23 other conditions, according to our data. His clinical expertise encompasses Acromicric Dysplasia, Split Hand Foot Malformation, X-Linked Spondyloepiphyseal Dysplasia Tarda, and Clouston Syndrome.
Can Kosukcu practices practicing medicine in Ankara, Turkey. Mr. Kosukcu is rated as an Experienced expert by MediFind in the treatment of Dihydrolipoamide Dehydrogenase Deficiency. He is also highly rated in 4 other conditions, according to our data. His clinical expertise encompasses Brachydactyly Type B, 3M Syndrome, Carnitine-Acylcarnitine Translocase Deficiency, and Short-Chain Acyl-CoA Dehydrogenase Deficiency.
Last Updated: 04/28/2026