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

An adult had a rare scalp infection in the forehead area, treated successfully with itraconazole.

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

The patient has frontal fibrosing alopecia (FFA).

Vogt-Koyanagi syndrome often leads to partial or complete blindness and responds poorly to treatment.

A rare skin condition with dark, thick, warty patches and some hair loss was found in a newborn boy.

The term "Porokeratotic Adnexal Ostial Nevus" is suggested as a more appropriate name.

A baby boy with 13q deletion syndrome had eye cancer, a woman's vision improved after stopping a breast cancer drug, a man developed cataracts from using Propecia, and a rare skin disorder called Lipoid Proteinosis was discussed. Also, a tool called OCT is useful for diagnosing macular diseases.

A young man with an unusual type of scarring hair loss suggests a possible new variant of a known scalp condition.

The boy's hair and skin color differences are due to a pigmentation disorder.

A 17-year-old girl and her brothers have a rare hair condition with long eyelashes, thick eyebrows, and easily pluckable hair.

Pressure-induced hair loss is rare, often reversible, and early diagnosis is crucial to prevent complications.

Lichen planopilaris mostly affects women with fair skin and can look different on each person, needing early treatment to prevent hair loss.

A young Caucasian man experienced a rare type of hair loss on the back of his head.

Four new cases confirmed the unique features of follicular porokeratosis.

A baby girl has a hair disorder called monilethrix, causing fragile hair that may improve over time.

The boy likely has a fungal infection causing hair loss.

Poliosis circumscripta is a patch of white hair caused by lack of melanin, linked to genetic and acquired conditions.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

Acitretin moderately improved skin and eye issues but not hair loss or light sensitivity in a 3-year-old with IFAP syndrome.

The report shows a young man with Hutchinson-Gilford Progeria Syndrome had typical and additional eye problems related to the disease.

Laser treatments are the most effective for porokeratotic adnexal ostial nevus.

Consider TFI in facial hypopigmentation diagnoses and confirm with a biopsy.

Pseudopelade is a rare inherited hair loss condition with a genetic cause.

Treatment with vitamin A did not improve the child's skin condition.

A child with Olmsted syndrome showed mild improvement in hair and skin issues with treatment.

Some people with lichen planus pigmentosus might later develop frontal fibrosing alopecia.

A Japanese patient with a rare genetic disorder had a less severe case than others, suggesting other factors may affect symptoms.