A CLINICAL CASE OF LARON SYNDROME IN THREE SIBLINGS

Laron syndrome (Laron dwarfism) is a rare genetic disease with an autosomal recessive type of inheritance caused by defects in the somatotropic hormone receptor gene (GHR gene), leading to insensitivity of peripheral tissues to growth hormone. Typical manifestations include low height, "doll fa...

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Main Authors: Яна Вячеславовна Юнкина (Author), Алла Дмитриевна Алексеева (Author), Галина Андреевна Поленчик (Author), Наталья Александровна Жданова (Author)
Format: Book
Published: The Publishing House Medicine and Enlightenment, 2022-11-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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