Search

everythinglearnresearchcommunity

for

Search:↓

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

The man's hair loss and skin papules were diagnosed as atrichia with papular lesions, not alopecia areata universalis.

An elderly woman's upper lip lump, thought to be a mucocele, was actually a rare type of lymphoma usually found on legs, treated successfully with chemotherapy and radiation.

Some people's hair turned white or gray after using intense pulsed light for hair removal, and for some, it was permanent.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

Early diagnosis and treatment of Lichen Planopilaris are crucial to prevent permanent hair loss.

Mutations in the hairless gene cause a rare form of permanent hair loss.

Lichen planus pigmentosus is hard to treat and may be more common in North Africa than previously thought.

A girl with Turner syndrome had psoriasis, alopecia areata, and trachyonychia.

A 7-year-old dog with a rare autoimmune disease was euthanized due to severe anemia and poor prognosis.

The patient has Chronic Cutaneous Lupus, a skin condition causing plaques and hair loss.

Trichodysplasia spinulosa can occur after a heart transplant due to immunosuppressive drugs.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

This rare genetic disorder causes permanent hair loss and skin bumps from birth.

Tumor cells in calcifying epithelioma of Malherbe resemble hair follicle cells.

Hair loss is a rare but recognized symptom of pemphigus vulgaris, with patients usually regrowing hair after treatment.

Two siblings had a rare hair condition with banded hair, which doesn't need treatment.

Removing both KLK5 and KLK7 proteins can prevent death and skin issues in Netherton syndrome.

Trichorrhexis nodosa is mainly caused by hair trauma and improves with gentler hair care.

Beau's lines on fingernails might indicate past severe COVID-19 and risk of reinfection.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

The case suggests a possible autoimmune link between lichen sclerosus and vitiligo.

Vigorous rubbing of herbal powder on the scalp caused hair damage and loss.

Early detection and multidisciplinary treatment are crucial for managing Papillon-Lefévre syndrome.

Early and accurate diagnosis is crucial for managing rare genetic disorders like this localized variant of junctional epidermolysis bullosa.

A man had both alopecia areata and lichen planus, which is uncommon.

A 9-year-old boy had a calcium deposit nodule on his earlobe.

Skin changes like hair loss, white patches, and nail changes are common in children after bone marrow transplants, often linked to chronic rejection.