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A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

Rapp-Hodgkin syndrome, AEC, and EEC are different expressions of the same genetic disorder caused by TP63 gene mutations.

Dermoscopy quickly and accurately diagnosed a rare hair disorder in a 12-year-old girl.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

The document suggests a possible link between FAM111B gene mutations and increased cancer risk, particularly pancreatic cancer.

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

The document concludes that Hidradenitis suppurativa is often underdiagnosed, lacks definitive treatment, and requires better awareness and management strategies.

Dermoscopy helps accurately diagnose temporal triangular alopecia, avoiding unnecessary treatments.

Melasma's causes include genetics, sun exposure, hormones, and oxidative stress, and understanding these can help create better treatments.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

Trichoscopy helps tell apart Frontal Fibrosing Alopecia and Lichen planopilaris by showing different hair and scalp features.

Some natural ingredients like onion juice, rosemary oil, and pumpkin seed oil may help with hair growth and reducing hair loss.

A woman with CCCA has hair loss due to factors like straighteners and tight hairstyles, and treatments include steroids and avoiding certain hair products.

Glucocorticoids for progressive muscular dystrophy in children don't improve muscle strength or function but do increase certain side effects.

Lipedema is a painful fat disorder in women that's hard to treat, often worsens with hormonal changes, and requires symptom-focused therapies.

The woman has a rare skin condition called follicular Dowling-Degos disease, which has limited treatment options.

Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.

A one-year-old cat had multiple benign skin tumors similar to those known in humans.

A baby had a rare case of widespread milia, which was treated and is being monitored.

A condition called Central Centrifugal Cicatricial Alopecia causes hair loss and scalp burning in middle-aged African women, and it's treated with various medications, hair transplants, and non-drug methods like wigs.

Nilotinib can cause generalized keratosis pilaris.

Ashwagandha may improve hormone levels and reduce hair loss in non-classical adrenal hyperplasia.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

Androgenetic alopecia, or hair loss, is caused by a mix of genetics, hormones, and environment, where testosterone affects hair growth and causes hair to become smaller and grow for a shorter time.

Hidradenitis suppurativa might be a type of autoinflammatory skin disease.

The document concludes that understanding genetic mutations in the PI3K-AKT-mTOR pathway can lead to better diagnosis and treatment for certain genetic skin disorders.

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

Bioengineering can potentially treat hair loss by regenerating hair follicles and cloning hair, but the process is complex and needs more research.