| Eponyms in category: Dystrophy |
| 24
main and alternative
entries found.
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| Batten's syndrome (Curschmann-Batten-Steinert syndrome) |
| Rare hereditary familial disease characterized by progressive muscular wasting, myotonia, cataracts, hypogonadism, and mental deterioration. |
| Batten-Gibb syndrome (Curschmann-Batten-Steinert syndrome) |
| Rare hereditary familial disease characterized by progressive muscular wasting, myotonia, cataracts, hypogonadism, and mental deterioration. |
| Batten-Steinert syndrome (Curschmann-Batten-Steinert syndrome) |
| Rare hereditary familial disease characterized by progressive muscular wasting, myotonia, cataracts, hypogonadism, and mental deterioration. |
| Batten-Turner form of congenital myopathy (Batten-Turner syndrome) |
| A benign form of congenital muscular dystrophy. |
| Batten-Turner syndrome |
| A benign form of congenital muscular dystrophy. |
| Batten’s disease (Curschmann-Batten-Steinert syndrome) |
| Rare hereditary familial disease characterized by progressive muscular wasting, myotonia, cataracts, hypogonadism, and mental deterioration. |
| Becker's dystrophy (Becker's muscular dystrophy) |
| A rare and relatively benign form of muscular dystrophy of pelvis-girdle type with better prognosis than Duchenne's dystrophy. |
| Becker's muscular dystrophy |
| A rare and relatively benign form of muscular dystrophy of pelvis-girdle type with better prognosis than Duchenne's dystrophy. |
| Becker's progressive muscular dystrophy (Becker's muscular dystrophy) |
| A rare and relatively benign form of muscular dystrophy of pelvis-girdle type with better prognosis than Duchenne's dystrophy. |
| Becker-Kiener muscular dystrophy (Becker's muscular dystrophy) |
| A rare and relatively benign form of muscular dystrophy of pelvis-girdle type with better prognosis than Duchenne's dystrophy. |
| Becker-Kiener syndrome (Becker's muscular dystrophy) |
| A rare and relatively benign form of muscular dystrophy of pelvis-girdle type with better prognosis than Duchenne's dystrophy. |
| Curschmann-Batten syndrome (Curschmann-Batten-Steinert syndrome) |
| Rare hereditary familial disease characterized by progressive muscular wasting, myotonia, cataracts, hypogonadism, and mental deterioration. |
| Curschmann-Batten-Steinert syndrome |
| Rare hereditary familial disease characterized by progressive muscular wasting, myotonia, cataracts, hypogonadism, and mental deterioration. |
| Curschmann-Steinert syndrome (Curschmann-Batten-Steinert syndrome) |
| Rare hereditary familial disease characterized by progressive muscular wasting, myotonia, cataracts, hypogonadism, and mental deterioration. |
| Curschmann-Steinert-Batten disease (Curschmann-Batten-Steinert syndrome) |
| Rare hereditary familial disease characterized by progressive muscular wasting, myotonia, cataracts, hypogonadism, and mental deterioration. |
| Duchenne's dystrophy in females |
| Typical clinical symptoms of Duchenne-Griesinger syndrome in females. |
| Duchenne-Becker muscular dystrophy, Becker type (Becker's muscular dystrophy) |
| A rare and relatively benign form of muscular dystrophy of pelvis-girdle type with better prognosis than Duchenne's dystrophy. |
| Erb's dystrophy |
| A slowly progressing, juvenile form of muscular dystrophy, affecting each sex equally. |
| Erb’s scapulohumeral dystrophy (Erb's dystrophy) |
| A slowly progressing, juvenile form of muscular dystrophy, affecting each sex equally. |
| Erb’s syndrome I (Erb's dystrophy) |
| A slowly progressing, juvenile form of muscular dystrophy, affecting each sex equally. |
| Rossolimo-Curschmann-Batten-Steinert myotinic dystrophy (Curschmann-Batten-Steinert syndrome) |
| Rare hereditary familial disease characterized by progressive muscular wasting, myotonia, cataracts, hypogonadism, and mental deterioration. |
| Rossolimo-Curschmann-Batten-Steinert syndrome (Curschmann-Batten-Steinert syndrome) |
| Rare hereditary familial disease characterized by progressive muscular wasting, myotonia, cataracts, hypogonadism, and mental deterioration. |
| Steinert’s disease (Curschmann-Batten-Steinert syndrome) |
| Rare hereditary familial disease characterized by progressive muscular wasting, myotonia, cataracts, hypogonadism, and mental deterioration. |
| Steinert’s myotonic dystrophy (Curschmann-Batten-Steinert syndrome) |
| Rare hereditary familial disease characterized by progressive muscular wasting, myotonia, cataracts, hypogonadism, and mental deterioration. |
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