Search

everythinglearnresearchcommunity

for

Search:↓

Folliculitis Decalvans and Frontal Fibrosing Alopecia can coexist in people with darker skin, showing features of both conditions.

Recognizing scalp symptoms in PRP is crucial for proper diagnosis and treatment.

Treatment with moisturizers improved the skin condition of a girl with a rare genetic skin disorder.

The Persian cat has a skin infection caused by a fungus, treatable with antifungal medication.

The gene therapy showed significant wound healing and was safe for treating severe RDEB.

The dog's skin and anemia issues returned after stopping treatment for Babesia gibsoni.

Frontal fibrosing alopecia can mimic traction alopecia but has distinct features like facial papules and eyebrow thinning.

Hair casts can be treated with physical removal and special shampoos.

A rare skin growth in a baby was successfully removed without coming back.

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

The report shows that a rare benign tumor was successfully removed from inside the mouth to avoid scarring on the face.

Bardet-Biedl syndrome may include under-recognized skin problems related to its metabolic disturbances.

Localized dystrophic epidermolysis bullosa (DEB) can lead to scarring alopecia, highlighting the need to recognize and address this complication.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.

The girl's "dandruff" was actually harmless hair casts, not a hygiene issue.

Plica neuropathica can be a sign of schizophrenia and improves with antipsychotic treatment.

An 8-year-old girl has a rare genetic disorder causing complete, irreversible hair loss and skin bumps.

Danon disease can be hard to diagnose due to non-specific symptoms.

PRAME is often present in Paget disease and could help in diagnosis, but more research is needed.

Lipedematous scalp may be underdiagnosed and doesn't improve with finasteride.

The treatment for alopecia areata with diphenylcyclopropenone was unsuccessful.

The pedicled temporoparietal fascial flap is a reliable and versatile option for reconstructive surgery in the head and neck area.

A person was born with both a rare hairless condition and a type of birthmark, which is an uncommon combination.

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.

A specific gene mutation causes a severe skin disorder in a family.

Pentoxifylline effectively improves pretibial pruritic papular dermatitis.

A new gene mutation linked to a skin condition was found in a Spanish family.

The woman likely has secondary syphilis, treatable with penicillin.

A woman with IgG/IgA pemphigus was treated successfully with dapsone and steroids.