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Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

A Saudi girl was diagnosed with Loose Anagen Hair Syndrome, a rare condition causing easy hair loss without scarring.

A patient with sickle cell trait and low vitamin D might have lupus, a rare combination that needs more attention.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

A 5-year-old girl has sparse, dry, and brittle hair but is otherwise healthy.

A 56-year-old man was diagnosed with Cronkhite-Canada Syndrome after showing symptoms like diarrhea, weight loss, and skin changes.

Acne is linked to inflammation and insulin resistance, and is associated with various syndromes that require different treatments.

Using old drugs for new uses can help treat rare immune deficiencies.

Children with classic congenital adrenal hyperplasia have thicker heart fat and more heart and blood vessel risk factors, especially if their condition is not well-controlled.

Patients often experience long-lasting changes to their hair after stem cell transplants.

Adjusting the medication tacrolimus resolved a boy's red nail beds after a stem cell transplant.

People with Down's syndrome are more likely to have syringomas.

Bovines can have rare inherited skin diseases with specific symptoms like hair loss, fragile skin, and abnormal porphyrin buildup.

Different nail disorders are treated by targeting their specific causes and using appropriate medications or protective measures.

Eating a lot of soy might lower the chance of early hair loss in men likely to get it.

Hormones, especially testosterone and DHT, are key for penis development and function, and testosterone therapy may help with erectile dysfunction in those with low levels.

Benzoyl peroxide and adapalene gels work differently to reduce acne in mice.

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

The document concludes that there are various causes and treatments for hair loss, with hair transplantation being a notable option.

Vitamin D3 and its receptor are important for hair growth, and understanding receptors could help treat hair graying and skin cancer.

Men with early hair loss may have a higher risk of enlarged prostate and possibly prostate cancer due to shared hormonal factors.

Many adult women experience unexplained excessive hair shedding, often starting before age 40.

Marie-Unna Hereditary Hypotrichosis is a rare genetic condition causing sparse hair growth, requiring specific recognition for proper care.

A 72-year-old man was diagnosed with a rare skin form of Rosai-Dorfman disease after years of misdiagnosis.

About 30% of women feel they lose too much hair, often starting before age 40, and most can't find a reason for it.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

Nonclassic congenital adrenal hyperplasia is a common genetic disorder that can cause a range of symptoms and requires personalized treatment.

Transverse sections are better for non-scarring hair loss, vertical sections are better for lichen planopilaris, and either method works for other scarring hair loss types.

Mutations in the P2RY5 gene cause hereditary woolly hair.