| infantile l. |
biliary cirrhosis of children; see under cirrhosis.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| infantile m. |
a condition present at birth or occurring soon after, characterized by the presence of solitary or multiple, firm, rubbery, spherical or ovoid nodules in the skin and subcutaneous tissues. The nodules are composed of myofibroblasts and may undergo ulceration and calcification. In about half of patients, skeletal fibromas also occur; when lesions are limited to the skin and bones (a condition sometimes known as congenital multiple fibromatosis), prognosis is good and lesions resolve spontaneously. Visceral involvement may also occur (congenital generalized fibromatosis, q.v.) and is highly lethal.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| infantile nephropathic c. |
early onset c.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| infantile neuroaxonal d. |
progressive hereditary degenerative encephalopathy transmitted as an autosomal recessive trait, beginning in infancy with muscular hypotonia and arrest of development in late infancy, followed by dementia, blindness, spasticity, and ataxia. Pathologically it is characterized by widespread focal swellings and degeneration of the axons with scattered spheroids in the brain. In some, but not all, cases it is caused by a deficiency of α-N-acetylgalactosaminidase. Called also Seitelberger's disease.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| infantile p. |
the major illness of poliomyelitis; see poliomyelitis.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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