| hereditary retinal a. |
amaurosis congenita.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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|---|---|
| hereditary s. |
a congenital, usually autosomal dominant form of spherocytosis with hemolytic anemia, abnormal fragility of erythrocytes, jaundice, and splenomegaly; it is the most common form of hereditary anemia among people of European descent. Called also congenital hemolytic or spherocytic anemia; chronic familial, congenital familial, or congenital hemolytic icterus; chronic acholuric or familial acholuric jaundice; and Minkowski-Chauffard syndrome.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| hereditary sensory and autonomic n. |
any of several inherited neuropathies that involve slow ascendance of lesions of the sensory nerves, resulting in pain, distal trophic ulcers, and a variety of autonomic disturbances. Some diseases in this group have been numbered: type I is the autosomal dominant form of hereditary sensory radicular neuropathy; type II is the autosomal recessive form of hereditary sensory radicular neuropathy; and type III is familial dysautonomia.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| hereditary sensory and motor n. |
hereditary motor and sensory n.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| hereditary sensory n. |
hereditary sensory radicular n.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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