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A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

A man with both Klinefelter syndrome and primary hyperparathyroidism showed a rare combination of symptoms and genetic patterns.

Certain gene variations are not a major cause of male infertility in Nigerian men.

Certain changes in the VEGF gene can increase or decrease the risk of polycystic ovary syndrome.

Swedish men with the E213 A-allele of the androgen receptor have a lower risk of prostate cancer.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

Genetic variations may affect how well finasteride works for BPH patients.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

A new gene mutation linked to a skin condition was found in a Spanish family.

Different forms of finasteride dissolve and remain stable differently, affecting capsule quality.

Certain gene variations in the Vitamin D receptor may increase the risk of chronic hair loss.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

Mutations in the enzyme don't significantly change how it binds to its specific substances.

SRD5A2 gene variations affect PTSD symptoms differently in males and females.

FGF13 gene changes cause excessive hair growth in a rare condition.

Researchers created a new mouse model, G4, that mimics human PCOS symptoms and links the condition to a specific gene.

Certain genetic variants may increase the risk of developing PCOS.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

Certain gene variations may increase the risk of hair loss in Egyptians.

Certain gene variants in estrogen receptors are linked to polycystic ovary syndrome, mainly affecting metabolism, in Tunisian women.

Microarray analysis helps find hidden chromosomal changes in patients with intellectual disabilities and birth defects.

Certain gene variations are found in people with polycystic ovary syndrome.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

Certain genetic variants impair enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.

The Tru9I variant in the VDR gene may influence alopecia areata risk and vitamin D levels.