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People with X-linked hypohidrotic ectodermal dysplasia have no sweat ducts and less, thinner hair.

Estrogens are key for bone growth spurts in both boys and girls and affect growth into adulthood.

Low-coverage sequencing is a cost-effective way to find genetic factors affecting rabbit wool traits.

The KRTAP21-1 gene affects wool yield and can help improve wool production.

Certain gene variations and different levels of BDNF and CRH hormones are linked to vitiligo.

Higher miR-34a levels and the A variant of the MIR-34A gene are linked to increased risk and severity of alopecia areata.

Certain gene variations in PITX2 are linked to a higher risk of male pattern baldness in Indians.

Damaging mutations in NFKB2 cause a severe and distinct form of primary immunodeficiency with early-onset and often ACTH-deficiency.

Genetic variation in the KRTAP15-1 gene affects wool yield in sheep.

Forensic DNA Phenotyping accurately predicts physical traits and is used in investigations, but needs more diverse population data for confirmation.

Genetic screening for NUDT15 polymorphisms is crucial for patients taking azathioprine, especially in Asians.

Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.

Four new cases of Bachmann-Bupp syndrome suggest potential for targeted treatment.

Androgen self-administration might be controlled by membrane receptors, not nuclear ones.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Understanding wool keratin-associated proteins in sheep can help improve wool quality through selective breeding.

Notch signaling is essential for healthy skin and hair follicle maintenance.

Hair protein analysis might help identify a person's ethnicity, sex, and age in forensics.

Autism's genetics are linked with early age of puberty and less hair loss, but not with hormone levels or polycystic ovary syndrome.

The Msx2 gene affects feather development in Hungarian white geese and a specific gene variation could indicate feather quality.

A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

Variant G of the KRTAP20-1 gene improves wool curliness in Chinese Tan sheep.

New microneedle treatment with growth factors and a hair loss drug shows better and faster hair growth results than current treatments.

Hair loss from Alopecia Areata is caused by both genes and environment, with several treatments available but challenges in cost and relapse remain.

Fat tissue stem cells may help increase hair growth.

Certain gene variations are linked to higher male hormone levels in Chinese women with PCOS and insulin resistance.

The rs231775 genetic variant is linked to a higher risk and severity of Alopecia Areata in males.

The we/we wal/wal mice have defects in hair growth and skin layer formation, causing hair loss, useful for understanding alopecia.

Polycystic ovary syndrome is a complex condition that affects women's mental, reproductive, and metabolic health throughout their lives.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.