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Mutations in the LSS gene cause hair loss and may affect brain development, with varying severity.

Pseudopelade is a rare inherited hair loss condition with a genetic cause.

Flutamide-induced hypospadias in rats slows down early wound healing.

People with hypohidrotic ectodermal dysplasia are more likely to experience long-term fatigue and hair loss after COVID-19.

The girl's swelling and skin issues improved with fluid restriction and diuretics.

A genetic mutation in the LIPH gene causes a rare hair disorder with sparse, curly hair.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

The new hydrogel helps heal diabetic wounds by reducing inflammation and improving tissue repair.

Alopecia areata may be linked to kidney issues, but more research is needed.

Harlequin ichthyosis involves abnormal skin cell structures and giant mitochondria, affecting skin and hair.

A 15-year-old with KID syndrome developed a rare skin condition called PEHFN.

Hutchinson-Gilford Progeria Syndrome caused rapid aging due to a genetic mutation, with treatments to manage symptoms.

THA is a rare condition with no significant clinical consequences if thyroid function is normal.

Erosive pustular dermatosis of the scalp causes painful, scarring skin lesions on the scalp, mainly in elderly people with sun-damaged skin.

Gomez–Lopez–Hernandez syndrome can cause focal hair loss and developmental delays but some children can still function well and excel in school and sports.

Hair loss in a drug reaction case involved both a common shedding phase and an immune attack on hair follicle stem cells.

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

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

Older parental age, rural living, and specific genetic mutations increase hypospadias risk in children.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

Trichoscopy can reveal specific hair and scalp changes in linear morphea.

A gene mutation in mice causes increased mast cells and disorganized hair follicles in their skin.

Restoring EDA and WNT pathways early may help improve skin, hair, and teeth issues in hypohidrotic ectodermal dysplasia.

Faulty Notch signalling may cause hair follicle changes and inflammation in hidradenitis suppurativa.

A new DSG4 gene mutation causes hair defects in a young girl.

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

Hair loss and aging are caused by the breakdown of a key protein in hair stem cells.

The junction of the inner and outer prepuce with good blood flow is best for vascular pedicle flaps.

A woman with childhood growth hormone deficiency had multiple hormone deficiencies and developed serious lung and kidney problems later in life.

A 12-year-old boy in rural south India had a rare skin condition causing hair loss and inability to sweat.