Crandall syndrome

Cran·dall syn·drome

(kran'dăl), [MIM*262000] characterized by pili torti, sensorineural deafness, and hypogonadism; a familial trait in which there is a deficiency of luteinizing and of growth hormone.
See also: Björnstad syndrome.

Cran·dall syn·drome

(kran'dăl sin'drōm) Characterized by pili torti, sensorineural deafness, and hypogonadism; a familial trait in which there is a deficiency of luteinizing and growth hormones.
See also: Björnstad syndrome

Crandall,

Barbara F., U.S. pediatrician. Crandall syndrome - recessive trait causing deafness, baldness, and hypogonadism.

单词	crandall syndrome
释义	Crandall syndrome Cran·dall syn·drome (kran'dăl), [MIM262000] characterized by pili torti, sensorineural deafness, and hypogonadism; a familial trait in which there is a deficiency of luteinizing and of growth hormone. See also: Björnstad syndrome. Cran·dall syn·drome (kran'dăl sin'drōm) Characterized by pili torti, sensorineural deafness, and hypogonadism; a familial trait in which there is a deficiency of luteinizing and growth hormones. See also: Björnstad syndrome Crandall, Barbara F., U.S. pediatrician. Crandall syndrome* - recessive trait causing deafness, baldness, and hypogonadism.
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