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Over a third of women thought to have non-classical congenital adrenal hyperplasia didn't have it confirmed by genetic tests.

A pregnant woman with Werner's syndrome died during childbirth, but her baby survived and did not have the syndrome.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

The document concludes that individuals with a rare genetic disorder linked to the AEBP1 gene may experience a unique type of hair loss and should be monitored for heart issues.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

CaBP1 and 2 are important for maintaining the activity of calcium channels necessary for hearing in inner ear cells.

TRPV3 in skin cells causes inflammation and cell death.

sPLA2-X is crucial for normal hair growth and follicle health.

The document talks about hard-to-treat and rare acne types, their connection with other health issues, the importance of correct diagnosis, and the challenges in managing them.

Foxp3+ Regulatory T Cells are important for immunity and tolerance, affect hair growth and wound healing, and their dysfunction can contribute to obesity-related diseases and other health issues.

Narrowband UVB therapy significantly improved a child's rare skin condition.

Matriptase is highly active in hair follicles and sebaceous glands, especially during hair growth phases.

Overexpression of FGF5s makes Chinese Merino sheep grow longer and heavier wool.

A woman with lupus had muscle weakness due to kidney issues and was successfully treated with medication.

"D-CHRAMPS syndrome" is a newly identified condition with multiple severe symptoms.

Zinc is crucial for skin health and treating various skin disorders.

Imaging helps detect adrenal gland issues and monitor treatment in congenital adrenal hyperplasia, and can identify tumors affecting fertility.

Significant progress and collaborations in stem cell research and regenerative medicine were made, including advancements in hair growth, cancer therapies, and treatments for neurological disorders.

Abnormal gene expression related to keratin causes hair loss in certain mice.

Androgen treatment with dihydrotestosterone may help maintain height in patients with 5-α-reductase type 2 deficiency, especially before puberty.

A baby with a skin condition improved with treatment but developed a rare form of the condition affecting only his trunk.

Monilethrix causes different levels of hair loss in family members.

Monilethrix causes fragile, patchy hair loss.

Methylene blue is less effective than normal saline solution for storing hair grafts and may reduce graft survival.

The JAK/STAT pathway is important in cell processes and disease, and JAK inhibitors are promising for treating related conditions.

Ectodysplasin inhibits Wnt signaling to help form hair follicles.

Trichoscopy is a quick and easy way to diagnose most genetic hair problems without invasive methods.

Vitamin D receptor is crucial for bone health and mineral metabolism.

Future hair cosmetics will be safer and more effective.