MediFind found 6 doctor with experience in Mucopolysaccharidoses (MPS) near Gifu, JP. Of these, 3 are Distinguished and 3 are Experienced.
Tadao Orii practices in Gifu-shi, Japan. Mr. Orii is rated as a Distinguished expert by MediFind in the treatment of Mucopolysaccharidoses (MPS). His top areas of expertise are Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome), Mucopolysaccharidoses (MPS), Mucopolysaccharidosis Type 4A (MPS IVA, Morquio Syndrome Type A), Osteotomy, and Bone Marrow Transplant.
Kenji Orii practices in Gifu-shi, Japan. Mr. Orii is rated as a Distinguished expert by MediFind in the treatment of Mucopolysaccharidoses (MPS). His top areas of expertise are Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome), Mucopolysaccharidoses (MPS), Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome), Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome), and Bone Marrow Transplant.
Toshiyuki Fukao practices in Gifu-shi, Japan. Mr. Fukao is rated as a Distinguished expert by MediFind in the treatment of Mucopolysaccharidoses (MPS). His top areas of expertise are Gorham's Disease, Skeletal-Extraskeletal Angiomatosis, Beta-Ketothiolase Deficiency, Lymphangiomatosis, and Bone Marrow Transplant.
Hidenori Ohnishi practices in Gifu-shi, Japan. Ohnishi is rated as an Experienced expert by MediFind in the treatment of Mucopolysaccharidoses (MPS). Their top areas of expertise are Cavernous Lymphangioma, Ectodermal Dysplasias, Clouston Syndrome, and Aplasia Cutis Congenita.
Akitaka Shibata practices in Tajimi, Japan. Shibata is rated as an Experienced expert by MediFind in the treatment of Mucopolysaccharidoses (MPS). Their top areas of expertise are Lamellar Ichthyosis, Fetal Retinoid Syndrome, Nonbullous Congenital Ichthyosiform Erythroderma, and Harlequin Ichthyosis.
Hideki Matsumoto practices in Gifu-shi, Japan. Mr. Matsumoto is rated as an Experienced expert by MediFind in the treatment of Mucopolysaccharidoses (MPS). His top areas of expertise are Pseudoachondroplasia, Craniometaphyseal Dysplasia, Beta-Ketothiolase Deficiency, and Pyle Disease.
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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: 01/09/2026