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A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

Certain genetic variants reduce enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

Certain genetic variants impair enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

A rare genetic mutation causes resistance to vitamin D, leading to severe rickets and requiring high doses of calcium and vitamin D for treatment.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

Trichoscopy can diagnose monilethrix, a genetic hair defect causing hair thinning and loss.

Oral minoxidil and growth factors improved hair density and thickness in a girl with hereditary hair loss.

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

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

English springer spaniels are more prone to severe sebaceous adenitis than standard poodles.

Hair growth and health are influenced by factors like age, environment, and nutrition, and are controlled by various molecular pathways. Red light can promote hair growth, and understanding these processes can help treat hair-related diseases.

Key genes crucial for sheep hair follicle development were identified, aiding fine wool breeding and human hair loss research.

Zinc is important for skin health, and supplements can help treat various skin and hair disorders, but more research is needed for conditions like psoriasis and vitiligo.

Zinc is crucial for skin health and treating various skin disorders.

Poor nutrition can lead to skin diseases in hospitalized patients and should be quickly identified and treated.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

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

The ABCA4 gene protects hair follicle stem cells from toxic vitamin A byproducts.

Premature aging increases the risk of immune problems and autoimmune diseases.

Botanical extracts and Minoxidil improved hair condition in a boy with a genetic disorder.

HOXC13 is essential for hair and nail development by regulating Foxn1.

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

AE can have varied symptoms and genetic causes, but zinc therapy helps.

Some children in Malaysia with symptoms have either profound or partial biotinidase deficiency, and early testing and treatment are important.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

Advances in genetics may lead to targeted treatments for hair disorders.

Genetic variations greatly affect individual metabolism and can impact health and disease risk.

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

A woman with acne and baldness was found to have a rare ovarian condition but successfully had a child through fertility treatment.

A patient with Werner syndrome showed a range of aging-like symptoms and metabolic issues, underscoring the need for early detection and treatment.