Medical Definition of Type I acrocephalosyndactyly

1. A usually inherited disorder characterised by premature closing of the cranial suture lines resulting in a peaked shaped head and abnormal facial appearance. Since it is usually autosomal dominant one or both parents also have the disorder. Surgery is used to correct skull and facial abnormalities. Inheritance: autosomal dominant. (29 Dec 1997)

Lexicographical Neighbors of Type I Acrocephalosyndactyly

type II dip
type II error
type II errors
type II familial hyperlipoproteinaemia
type II hyperlipoproteinaemia
type II interferon
type II mortality
type II mucopolysaccharidosis
type IS mucopolysaccharidosis
type IV allergic reaction
type IV familial hyperlipoproteinaemia
type IV prepilin peptidase
type I H/S mucopolysaccharidosis
type I acrocephalosyndactyly (current term)
type I allergic reaction
type I cells
type I collagen
type I diabetes
type I diabetes mellitus
type I dip
type I error
type I errors
type I familial hyperlipoproteinaemia
type I hyperlipoproteinaemia
type I interferon
type I mortality
type O
type VIII mucopolysaccharidosis

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