MediFind found 7 doctor with experience in Johanson-Blizzard Syndrome near Inner Mongolia, CN. Of these, 5 are Advanced and 2 are Distinguished.
Yi Liu practices in Jinan, China. Liu is rated as a Distinguished expert by MediFind in the treatment of Johanson-Blizzard Syndrome. Their top areas of expertise are Ectodermal Dysplasia Neurosensory Deafness, Johanson-Blizzard Syndrome, Nicolaides-Baraitser Syndrome, and Ring Chromosome 18.
Min Gao practices in Jinan, China. Gao is rated as a Distinguished expert by MediFind in the treatment of Johanson-Blizzard Syndrome. Their top areas of expertise are Ectodermal Dysplasia Neurosensory Deafness, Johanson-Blizzard Syndrome, Nicolaides-Baraitser Syndrome, and Dihydrolipoamide Dehydrogenase Deficiency.
Xuxia Wei practices in Jinan, China. Wei is rated as an Advanced expert by MediFind in the treatment of Johanson-Blizzard Syndrome. Their top areas of expertise are Ectodermal Dysplasia Neurosensory Deafness, Johanson-Blizzard Syndrome, Dubin-Johnson Syndrome, and Rotor Syndrome.
Zhongtao Gai practices in Jinan, China. Gai is rated as an Advanced expert by MediFind in the treatment of Johanson-Blizzard Syndrome. Their top areas of expertise are Continuous Spike-Wave During Slow Sleep Syndrome, Ornithine Transcarbamylase Deficiency, Ring Chromosome 18, and Dihydrolipoamide Dehydrogenase Deficiency.
Guohua Liu practices in Jinan, China. Liu is rated as an Advanced expert by MediFind in the treatment of Johanson-Blizzard Syndrome. Their top areas of expertise are Ectodermal Dysplasia Neurosensory Deafness, Johanson-Blizzard Syndrome, Imperforate Anus, and GM1 Gangliosidosis.
Yuqiang Lyu practices in Jinan, China. Lyu is rated as an Advanced expert by MediFind in the treatment of Johanson-Blizzard Syndrome. Their top areas of expertise are Ring Chromosome 18, Ring Chromosome 4, Citrullinemia, and Hennekam Syndrome.
Haiyan Zhang practices in Jinan, China. Zhang is rated as an Advanced expert by MediFind in the treatment of Johanson-Blizzard Syndrome. Their top areas of expertise are Dihydrolipoamide Dehydrogenase Deficiency, Maple Syrup Urine Disease, Carbamoyl Phosphate Synthetase 1 Deficiency, and Ornithine Transcarbamylase Deficiency.
Last Updated: 01/09/2026