The 20 Best Mucopolysaccharidoses (MPS) Doctors Near Me in Kumamoto, JP
Find the Top Mucopolysaccharidoses (MPS) Experts and Specialists
Kimitoshi Nakamura practices practicing medicine in Kumamoto, Japan. Nakamura is rated as an Advanced expert by MediFind in the treatment of Mucopolysaccharidoses (MPS). They are also highly rated in 18 other conditions, according to our data. Their clinical expertise encompasses Fabry Disease, Urea Cycle Disorders (UCD), Ornithine Transcarbamylase Deficiency, Vitrectomy, and Liver Transplant.
Takaaki Sawada practices practicing medicine in Kumamoto, Japan. Sawada is rated as an Experienced expert by MediFind in the treatment of Mucopolysaccharidoses (MPS). They are also highly rated in 5 other conditions, according to our data. Their clinical expertise encompasses Fabry Disease, Pompe Disease, Opisthotonos, and Argininosuccinic Aciduria.
Jun Kido practices practicing medicine in Kumamoto, Japan. Mr. Kido is rated as an Experienced expert by MediFind in the treatment of Mucopolysaccharidoses (MPS). He is also highly rated in 14 other conditions, according to our data. His clinical expertise encompasses Urea Cycle Disorders (UCD), Argininosuccinic Aciduria, Carbamoyl Phosphate Synthetase 1 Deficiency, Citrullinemia, and Liver Transplant.
Keishin Sugawara practices practicing medicine in Kumamoto, Japan. Sugawara is rated as an Experienced expert by MediFind in the treatment of Mucopolysaccharidoses (MPS). They are also highly rated in 6 other conditions, according to our data. Their clinical expertise encompasses Urea Cycle Disorders (UCD), Citrullinemia, Carbamoyl Phosphate Synthetase 1 Deficiency, Argininosuccinic Aciduria, and Liver Transplant.
Shirou Matsumoto practices practicing medicine in Kumamoto, Japan. Matsumoto is rated as an Experienced expert by MediFind in the treatment of Mucopolysaccharidoses (MPS). They are also highly rated in 7 other conditions, according to our data. Their clinical expertise encompasses Urea Cycle Disorders (UCD), Carbamoyl Phosphate Synthetase 1 Deficiency, Ornithine Transcarbamylase Deficiency, Argininosuccinic Aciduria, and Liver Transplant.
To see more doctors, please expand your search radius or view related conditions below.
Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome), Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome), Mucopolysaccharidosis Type 3 (MPS III, Sanfilippo Syndrome), Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome)
Last Updated: 04/28/2026