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Using 17-hydroxyprogesterone levels to diagnose nonclassic congenital adrenal hyperplasia can result in many incorrect diagnoses.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

A blood test level of 3.2 ng/mL of Antimüllerian hormone is good for identifying polycystic ovarian morphology in European women aged 25–45.

Substance from human umbilical cord blood cells promotes hair growth.

EDA signaling is linked to skin disorders, various cancers, and liver disease.

The HG3 hair gel is the most effective for treating seborrheic dermatitis.

CCCA is a scarring hair disorder mainly affecting people of African descent, needing better awareness and treatment.

Genetic mutations linked to ectodermal dysplasias and hair loss were identified in Pakistani families.

Mice without the vitamin D receptor gene lose hair due to disrupted hair follicle cycles.

A new AIRE gene mutation causes rare autoimmune symptoms in a Lebanese boy.

A new mouse model helps study melanocyte cells using GFP expression.

A new genetic model may improve treatment and diagnosis for certain inherited skin diseases.

CLK1 is needed for skin cells to become epidermal cells but not sebocytes.

Dermal Wnt/β-catenin signaling is important for the proper size and development of hair follicles.

Patients with central centrifugal cicatricial alopecia benefit from shared decision-making with their doctors.

Placental cell medium boosts blood vessel growth in lab tests.

The BUZZ gene is important for root hair growth and overall root structure in the plant Brachypodium distachyon.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

A faulty KLHL24 gene leads to hair loss by damaging hair follicle stem cells.

A specific gene variant may increase the risk of developing Alopecia Areata.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

Blocking 11β-HSD1 can lessen the harmful effects of glucocorticoids on hair growth cells.

AMH levels can't reliably tell the difference between LOCAH and all types of PCOS in women with excessive hair growth.

ODC transgenic mice can model human hair loss with skin lesions.

The ID2 gene can help distinguish between sensitizers and irritants in skin cells.

DNA methylation likely doesn't cause different lambskin patterns in Hu sheep.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

A form of vitamin E promotes hair growth by activating a specific skin pathway.