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Non-classical 21 hydroxylase deficiency is an underdiagnosed cause of female hair loss and polycystic ovarian syndrome.

The baby’s hair loss was due to a rare genetic condition, not treatable by usual methods.

Histone demethylases play a key role in the development of many diseases and may be targets for treatment.

The meeting highlighted major advances in skin research, including new findings on skin microbes, genetic links to skin diseases, and improved treatments for various conditions.

VEGF helps squamous cell carcinoma grow in ways beyond just blood vessel formation.

A girl with a rare skin condition improved after one month of treatment with acitretin.

Haircuts and medical growth factors do not cause cancer.

Malignant melanoma is the deadliest skin cancer, while BCC is the most common but rarely spreads, and SCC is more aggressive than BCC.

Young women in West Bengal, India, with PCOS often have estrogen resistance, leptin receptor issues, folate deficiency, T2DM, and acanthosis, commonly linked to obesity.

Minoxidil treatment improves heart defects in a DiGeorge syndrome model.

Disrupting natural body clocks increases the risk of developing type 2 diabetes.

Minoxidil improved hair growth in a child with a rare genetic disorder.

The review shows that skin symptoms like chronic fungal infections, hair loss, and skin depigmentation are key for early detection and management of APECED.

The enzyme Rand protease works well for leather dehairing and its stability is important, with Leu75 playing a key role.

Netherton syndrome can cause severe dehydration, infections, and growth issues in infants.

Different sebaceous gland diseases can be treated with medications, hormone therapy, or surgical methods.

Different people show different symptoms for genetic diseases because of how sensitive their bodies are to small changes in important factors.

The Arabidopsis rhd2 mutant is more sensitive to drought because of changes in cell membrane proteins and cell structure.

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

Impaired ABCA5 activity disrupts cholesterol balance in hair follicle cells, affecting hair growth.

An 11-year-old child with total hair loss may have a genetic autoimmune disease, and the outlook for hair regrowth is not good.

Tet2 and Tet3 enzymes are important for controlling hair growth and shape by affecting gene activity and DNA structure in hair follicles.

People with Collagen VI-related myopathies may often have hair loss and scalp issues.

Genetic testing confirmed a rare skin disorder in a young girl, which improved with zinc supplementation.

Stem cells from whiskers can be transplanted to stimulate hair growth.

The man has a genetic skin condition called pachyonychia congenita.

Understanding genetics is crucial for treating heart and skin diseases.

A girl with a rare skin condition called Keratosis Follicularis Spinulosa Decalvans showed no significant improvement with treatment.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

KIF18B is important for correctly positioning cell division machinery in skin cells, affecting hair follicle development.