Rossolimo-Steinert-Kurschmann dystrophic myotonia - analogs
| Description «Rossolimo-Steinert-Kurschmann dystrophic myotonia» | ||||||
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- 61% Compare Myotonic syndrome in children
- 59% Compare Progressive Erba-Roth muscular dystrophy
- 59% Compare Progressive Dreyfus muscular dystrophy
- 55% Compare Progressive Duchenne muscular dystrophy
- 53% Compare Becker 's Myotonia
- 50% Compare Oculopharyngeal muscular dystrophy
- 48% Compare Sluggish child syndrome
- 48% Compare Thomsen 's Myotonia
- 47% Compare Progressive bulbar paralysis
- 40% Compare MELAS syndrome
- 35% Compare Myopathic laryngeal paresis
- 32% Compare Steroid myopathy
- 30% Compare Neuromyotonia
- 28% Compare Small anomalies of heart development
- 28% Compare Septooptic dysplasia
- 28% Compare Pseudobulbar dysarthria
- 27% Compare Myofibrillary myopathy
- 27% Compare Terminal states
- 27% Compare E76 Disorders of glycosaminoglycan metabolism
- 26% Compare Alternating syndromes
- 25% Compare Distal motor neuropathy
- 24% Compare Neuropathic laryngeal paresis
- 24% Compare Tetanus in children
- 24% Compare Mowgli syndrome
- 24% Compare Charcot-Marie-Tuta neural amyotrophy
- 24% Compare Goldenhar syndrome
- 23% Compare Bulbar dysarthria
- 22% Compare MERRF syndrome
- 22% Compare Gurler syndrome
- 22% Compare I63.9 Cerebral infarction, unspecified
- 22% Compare Lawrence-Moon-Beadle syndrome
- 21% Compare Pallister-Killian syndrome
- 21% Compare I64 Stroke, not specified as haemorrhage or infarction
- 21% Compare Синдром Клиппеля–Треноне
- 21% Compare Malignant hyperthermia
- 21% Compare Locked-in syndrome
- 21% Compare Polymorbidity
- 21% Compare Pulmonary artery aneurysm
- 21% Compare Metabolic myopathy
- 21% Compare Feto-fetal transfusion syndrome
- 21% Compare Weak sinus node syndrome
- 20% Compare Galen's vein aneurysm
- 20% Compare Nitrate poisoning
- 20% Compare Uveitis in children
- 20% Compare Alien hand syndrome
- 20% Compare Acoustic-mnestic aphasia
- 20% Compare Stroke in children
- 20% Compare Hunter syndrome
- 20% Compare Polycythemia in newborns
- 20% Compare Friedreich 's familial ataxia
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