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...
Kaydedildi:
| Asıl Yazarlar: | , , , |
|---|---|
| Materyal Türü: | Kitap |
| Baskı/Yayın Bilgisi: |
The Publishing House Medicine and Enlightenment,
2022-11-01T00:00:00Z.
|
| Konular: | |
| Online Erişim: | Connect to this object online. |
| Etiketler: |
Etiketle
Etiket eklenmemiş, İlk siz ekleyin!
|
Internet
Connect to this object online.3rd Floor Main Library
| Yer Numarası: |
A1234.567 |
|---|---|
| Kopya Bilgisi 1 | Kütüphanede |