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Effective treatment guidelines for frontal fibrosing alopecia are still unclear.

Trichoscopy shows hair diameter variability, vellus hairs, and the peripilar sign are key indicators for diagnosing Androgenetic Alopecia.

Using animal names for skin conditions helps with learning and memory.

The document concludes that understanding hair follicle histology and the hair cycle is crucial for diagnosing alopecia.

The study concluded that Frontal fibrosing alopecia can affect younger people, is often missed in men, and may be autoimmune-related.

Thyroid disease can cause skin, hair, and nail problems, and treating the thyroid condition often improves these symptoms.

A woman's progressive hair loss was correctly diagnosed as a rare condition called fibrosing alopecia in a pattern distribution after initially being mistaken for a more common type.

The man has a genetic skin condition called pachyonychia congenita.

Oral minoxidil helps with hair growth but needs more research to fully understand its effectiveness and safety.

People with diabetes have a higher risk of skin infections and complications.

Monilethrix causes fragile, patchy hair loss.

Trichoscopy is crucial for diagnosing and managing androgenetic alopecia, showing increased vellus hairs, empty follicles, and fibrosis with severity.

Trichoscopy helps quickly identify autoimmune diseases on the scalp but should be used with other standard tests.

Low-dose oral isotretinoin improved hair loss and facial bumps in patients with a specific type of hair loss.

Trichoscopy is a useful tool for diagnosing hair and scalp diseases without needing skin biopsies.

Using combined treatments can help manage acne by targeting the bacteria and skin changes that cause it.

The study found that males with KFSD had severe skin and eye symptoms, while female carriers had milder symptoms.

A man with scalp and neck skin issues improved after a year of oral isotretinoin.

Connexin-26 gene mutations may increase cancer risk in KID syndrome patients.

Keratosis Follicularis Spinulosa Decalvans is a rare genetic disorder causing skin and hair issues, often inherited through the X chromosome.

A rare case of severe scalp hair loss and nail issues in keratosis follicularis was observed.

Substance P may play a role in the inflammation seen in keratosis follicularis spinulosa decalvans.

A 19-year-old man had a rare skin condition on one side of his face that looked like another skin disease.

Keratosis pilaris is a common skin condition causing a bumpy texture, sometimes linked to other diseases, with various treatments available.

Some canine hair follicle tumors contain amyloid deposits, with a protein called CK5 involved in their formation.

KFSD causes scarring hair loss and skin roughness, mainly in males.

The study concluded that key signs of Keratosis follicularis spinulosa decalvans are changes in terminal hair and vellus hair follicles, which likely start the inflammation and damage to hair follicles.

Keratosis pilaris is a common skin condition where hair follicles get clogged with keratin, mostly on the arms and thighs.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

Actinic keratosis can lead to skin cancer, is more common in fair-skinned people, and can be reduced with sunscreen and treated effectively.