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A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

Lower growth factors linked to balding in androgenetic alopecia.

The new bariatric surgery SAGI PGP is effective for weight loss and diabetes control with few complications.

A new gene mutation may allow some piebaldism patients to regain skin color in white patches.

Low oxygen levels affect the behavior of certain proteins in human skin cells.

A new genetic mutation was found causing hair and eye issues in a boy.

Sacituzumab Govitecan is effective for certain breast cancers but requires careful management of side effects.

A stable, active version of a growth factor was made in bacteria, showing promise for medical use.

Sgk3 kinase is essential for normal hair growth in mice.

CRABP1 boosts hair cell growth in Hu sheep by affecting key genes.

Disrupting a specific protein's function in hair follicle stem cells triggers their activation and a self-healing process.

A specific gene mutation causes sparse, brittle hair in a family.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

Jumonji genes are important for development and their mutations can cause abnormalities, especially in the heart and brain.

Defective mitochondrial DNA replication causes aging symptoms and increased oxidative damage in mice.

A 13-year-old boy with a rare genetic condition survived a heart attack and improved with treatment.

Future research on ectodysplasin should explore its role in diseases, stem cells, and evolution, and continue developing treatments for genetic disorders like hypohidrotic ectodermal dysplasia.

The research showed that Vitamin D and its receptor are important for healthy bones and normal hair and skin in rats.

Trichothiodystrophy is a rare genetic disorder causing hair issues and sometimes linked to DNA repair defects.

cDermo-1 causes dense skin, feathers, and scales in chickens.

Childhood and adult height, and early immune-related hospitalizations increase testicular cancer risk, while baldness, larger families, and sports reduce it.

Targeting ornithine decarboxylase can help prevent skin cancer.

THSG from a Chinese plant helps with aging and related diseases.

Patients with Bohring-Opitz syndrome and ASXL1 mutations need regular kidney ultrasounds to check for tumors.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.

Early diagnosis and a strict gluten-free diet are crucial for children with celiac disease to improve symptoms.

HDAC inhibitors help brain cells grow and improve brain function.

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

Cupric chloride treatment corrected abnormal Purkinje cell development in brindled mice.