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Higher hs-CRP levels in Indian adolescent women with PCOS are more related to BMI than PCOS itself.

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

Cronkhite-Canada syndrome causes chronic diarrhea and has a poor prognosis despite treatment.

Small molecules KY19382 and KY19334 may help treat skin cancer by reducing CDK1 levels and blocking harmful cell signals.

ExoFlo is safe and effective for treating Complex Regional Pain Syndrome symptoms.

CCCA causes progressive hair loss in Black women, starting from a central scalp patch.

Blocking CRF1 receptors improved male hormone levels and reduced testicular tumor size in men with a specific adrenal condition.

150 kHz electromagnetic radiation might help improve PCOS in rats.

CaM7 and CNGC14 interaction controls root hair growth in Arabidopsis.

A new syndrome, Teelwani Syndrome, combines features of two rare genetic disorders.

A rare gene variant causes sexual development issues in siblings, needing personalized treatment.

The project improved provider knowledge about PCOS but didn't significantly change diagnosis and management practices.

A five-month-old boy with Omenn syndrome successfully recovered after a stem cell transplant with reduced intensity conditioning.

Understanding factors affecting recurrence and survival can improve treatment for head and neck skin cancer.

Lhx2 is essential for effective Sonic Hedgehog signaling in early retinal development.

Patients with RASopathies are at risk for autoimmune disorders and should be routinely screened.

The U.K. created the CPSA to set safety standards for non-surgical cosmetic treatments and improve patient protection.

Disrupting β-catenin signaling in certain cells causes anorectal malformations.

Three siblings with a genetic form of rickets showed different symptoms of the disease.

Hair loss in Cronkhite-Canada syndrome may be due to an autoimmune response.

The search scheme SMRI is faster and more secure for retrieving encrypted data from the cloud.

The International Society of Hair Restoration Surgery created a standard curriculum in 2008 to guide doctors in diagnosing and treating hair loss effectively.

Sweat gland stem cells help maintain glands, aid wound healing, and can regenerate skin structures.

Low-dose Ritlecitinib may help children with stubborn Alopecia Areata.

Li2CO3 improved skin disease in a mouse model of Focal Dermal Hypoplasia without toxicity.

Krox20 (Egr2) is important for the function of epithelial stem cells.

Dual TCR Treg cells are common in various mouse tissues and show diverse characteristics.

Connexin-26 gene mutations may increase cancer risk in KID syndrome patients.

CARASIL, a rare genetic disorder, was confirmed in an Arabic woman, highlighting its rarity and need for stroke prevention.

The tool iCOUNT helps understand how stem cells divide and affect tissue development and repair.