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Combining genetic and physical trait analysis improves diagnosis accuracy for monogenic diabetes.

Testosterone undecanoate safely and effectively increased penis size in male children with 5-alpha-reductase deficiency.

A 15-year-old girl with no menstrual period was diagnosed with a genetic condition that makes her body unable to respond to male hormones, leading to female characteristics despite having male genetic makeup.

A child with trichothiodystrophy also had autoimmune thyroiditis and anemia, which is a new finding.

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

Knocking out certain genes in mice helps understand skin and hair growth problems.

Oral retinoic acid effectively treated collodion baby, with hair loss as the main side effect.

A new therapy for a skin blistering condition has not been developed yet.

Trichoscopy helps accurately diagnose Netherton syndrome, often mistaken for atopic dermatitis.

Treg cell-based therapies might help treat hair loss from alopecia areata, but more research is needed to confirm safety and effectiveness.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

Baricitinib reduces inflammation and improves cell health in premature aging cells.

New method finds genetic links between Type 2 Diabetes and Prostate Cancer not seen before.

Studying premature aging syndromes helps understand human aging and suggests potential treatments.

Rapamycin reduces age-related hearing cell loss in mice, but acarbose does not.

The genes KRT25 and SP6 affect curly hair in horses, with KRT25 also causing hair loss. If both genes are mutated, the horse gets curly hair and hair loss. KRT25 can hide the effect of SP6.

Wnt/β-catenin signaling is important for keeping skin cell attachment structures stable.

Light/laser therapy can effectively increase hair density in some types of alopecia, especially androgenic alopecia and alopecia areata.

The patient was diagnosed with oral lichen sclerosus and needs long-term monitoring.

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

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

Increasing research diversity is key for better understanding and treating Parkinson's Disease.

Monilethrix causes different levels of hair loss in family members.

Zinc supplements and diet changes can effectively treat zinc deficiency and prevent complications.

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

Cornification is how skin cells die to form the protective outer layer of skin, hair, and nails.

New therapies are being developed that target integrin pathways to treat various diseases.

Future hair cosmetics will be safer and more effective.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

Early balding in young Indian men may indicate a higher risk of metabolic syndrome and potential heart disease.