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Hair ages and thins due to factors like inflammation and stress, and treatments like antioxidants and hormones might improve hair health.

Genetic testing can help diagnose skin conditions but needs more research for full effectiveness.

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.

The most common cause of hair loss in children is tinea capitis, followed by alopecia areata and telogen effluvium.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

The man was diagnosed with Cronkhite-Canada syndrome, a rare disorder with GI polyps, skin issues, hair loss, and nail problems.

Rituximab may be an effective treatment for Cronkhite-Canada syndrome with kidney disease.

Trichoscopy is a quick and easy way to diagnose most genetic hair problems without invasive methods.

Congenital triangular alopecia is a hair loss condition present from birth or early childhood with no effective treatment needed.

Frontal fibrosing alopecia is a challenging hair loss condition with no known cause or definitive treatment.

Six genetic conditions are often linked to complete scalp hair loss in children.

Fibroblasts are crucial for tissue repair and inflammation, and understanding them can help treat fibrotic diseases.

The absence of functional sebaceous glands causes hair follicle destruction and scarring alopecia.

Hair follicles are normally protected from the immune system, but when this protection fails, it can cause hair loss in alopecia areata.

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

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

Probiotics help reduce hair loss and increase hair growth in people with androgenic alopecia.

Skin changes are key for early diagnosis and treatment of rheumatic diseases.

Olfactory receptors found outside the nose may offer new treatments for diseases like cancer and help in wound healing and hair growth.

People with Myotonic Dystrophy type 1 are more likely to have certain skin conditions, but not more likely to get skin cancer.

Trichoepitheliomas can be hard to distinguish from other skin conditions and often start in teenage years.

People with myotonic dystrophy type 1 tend to develop basal cell carcinoma at a younger age but not more frequently than others.

Some skin diseases and their treatments can negatively affect male fertility.

Robotic hair transplantation with AI offers more reliable, precise, and efficient hair restoration.

A man with myotonic dystrophy type 1 had 28 skin cancers, suggesting a link between the disease and skin cancer, emphasizing the need for sun protection and regular skin checks.

Intermediate filaments are crucial for cell differentiation and stem cell function.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

Lamins are vital for cell survival, organ development, and preventing premature aging.

An 11-year-old girl with a rare skin disorder also had cornea issues and dry eye, needing careful management.