| lamellar c. |
a concentric opacity, broad or narrow, usually consisting of powdery white dots, affecting one lamella or zonule of an otherwise clear lens. This is the most common type of congenital cataract, and causes include hypocalcemia, hypoglycemia, galactosemia, and rubella. Called also zonular c.
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| lamellar d. of the newborn |
see collodion baby, under baby.
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| lamellar e. of newborn |
see collodion baby, under baby.
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| lamellar g. |
replacement of the superficial layers of an opaque cornea by a thin layer of clear cornea from a donor eye.
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| lamellar i. |
a congenital, chronic form of ichthyosis present at birth, inherited as an autosomal recessive trait, in which the affected infant is born encased in a collodionlike membrane (see collodion baby, under baby) that is soon shed, the skin then becoming covered with large, coarse scales with involvement of all of the flexures as well as the palms and soles. Universal erythroderma and pruritus are characteristic, and ectropion of variable degree is usually present. Formerly called nonbullous congenital ichthyosiform erythroderma.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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