| multiple neuroma |
Neurofibromatosis.
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| multiple c. deficiency |
an inherited aminoacidopathy correctable by biotin therapy and due to deficiency of either holocarboxylase synthetase or biotinidase, which causes deficiency of activity of the biotin-containing carboxylases (acetyl-CoA carboxylase, methylcrotonoyl-CoA carboxylase, propionyl-CoA carboxylase, and pyruvate carboxylase); it is characterized by metabolic ketoacidosis, organic aciduria, hyperammonemia, and variable manifestation of breathing difficulties, hypotonia, seizures, ataxia, alopecia, skin rash, and developmental delay. Urine contains organic acids characteristic of each individual carboxylase deficiency, particularly 3-hydroxyisovaleric acid. The neonatal form, due to deficiency of holocarboxylase synthetase, is apparently an autosomal recessive trait, often of earlier onset, and may progress rapidly to coma; the juvenile form, due to deficiency of biotinidase, is an autosomal recessive trait and is characterized additionally by sensorineural deafness and optic atrophy. See also the individual enzymes and propionicacidemia.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| multiple osteocartilaginous exostosis |
A hereditary growth disorder marked by the development of multiple exostoses, usually on the diaphyses of long bones near the epiphyseal lines. It causes irregular growth of the epiphyses and often secondary
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| multiple cone m. |
lateral condensation m.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| multiple point electrode |
Several sets of terminals providing for the use of several electrodes. SEE: multiterminal.
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