Research Topic · Peer-Reviewed

Gigantism Hermaphroditism

Syndrome Gigantism Hermaphroditism Syndrome (GHS) is a rare genetic condition that affects the development of an individual's physical characteristics. Symptoms may include excessive growth of the limbs, hands, and feet, as well as abnormal sexual organs and genitalia. This syndrome can be caused by mutations in tw…

📚 0 peer-reviewed articles cited 🔖 ISSN 3070-2313 🗓 Reviewed June 2026

Overview

Syndrome Gigantism Hermaphroditism Syndrome (GHS) is a rare genetic condition that affects the development of an individual's physical characteristics. Symptoms may include excessive growth of the limbs, hands, and feet, as well as abnormal sexual organs and genitalia. This syndrome can be caused by mutations in two different genes, the GHS1 and the GHS2 gene, located on chromosome 17. It is important to diagnose and treat GHS as early as possible, due to the potential mental and physical development issues that can result. While there is no cure for GHS, early diagnosis and treatment can help manage the symptoms and help lead to a better quality of life.

Research published in this journal

No peer-reviewed research on this exact topic has been published in Endocrinology And Hormones yet. Browse the journal →

Editorial oversight

Curated from peer-reviewed research published in Endocrinology And Hormones (ISSN 3070-2313).

Journal editorial board
Kamran Mahmood Ahmed Aziz · Saudi Arabia Guangzhen Hu · United States Alexander G. Obukhov · United States

This page summarises published research for orientation; it is not medical or professional advice.