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Some parents have a mild form of congenital adrenal hyperplasia without symptoms, and they usually don't need treatment.

Children and adults with Cushing's disease show different symptoms and males have more severe cases; surgery outcomes can be predicted by certain factors.

Coinheritance of BRCA2 and CYLD genes may lead to new treatment options for certain cancers.

Dimethylarsinic acid speeds up skin tumor growth in certain mice.

Upadacitinib can cause hypersensitivity that worsens ulcerative colitis symptoms.

CARB is a strong barrier in human hair that prevents dye penetration.

Overexpressing CtBP1 in skin cells causes skin and hair problems.

AD-derived keratinocytes effectively mimic inflammation in atopic dermatitis.

Potassium channel openers show promise for treating heart disease and other conditions, but more research is needed to fully understand their effects and safety.

A new protein, mK6irs, is found in specific hair layers and may help understand hair growth and diseases.

Deleting the MAD2L1 gene is tolerated in certain mouse cancer models.

Genetic variants in specific genes cause central centrifugal cicatricial alopecia.

Prompt treatment of inflammatory tinea capitis (kerion) is crucial to prevent scarring and hair loss.

CREB, a protein that can promote cancer traits, is controlled by β-catenin in skin cancer cells.

The protein CCN2 controls hair growth by affecting hair follicle formation and stem cell activity in mice.

Corin speeds up wound healing by helping skin cells move and grow.

Mutations in the PADI3 gene may cause central centrifugal cicatricial alopecia in women of African ancestry.

Early diagnosis and a multidisciplinary approach are crucial for children with Trichothiodystrophy and hidden learning disorders.

AcSDKP may help prevent skin and hair aging and promote their growth.

A hospital outbreak of catheter infections in calves was caused by a bacteria from a beef herd, leading to longer hospital stays, more drug use, and calf deaths.

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

New genetic mutations linked to rare skin disorders were found in three newborns.

The study created a mouse model to better understand hair follicle stem cells' role in hair growth and repair.

Advancements in understanding, diagnosing, and managing congenital adrenal hyperplasia have improved treatment and long-term outcomes.

KATP channel openers may cause peripheral edema by reducing lymphatic contractions and flow.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

A new classification for trichothiodystrophy helps identify genetic causes and potential treatments.

A rare genetic disease causes rickets and often hair loss in young children, which can improve with specific treatments.

Epidermolytic ichthyosis can be inherited in a semidominant way with mild symptoms in carriers.