Search

everythinglearnresearchcommunity

for

Search:↓

The PROCLIPI study found markers that help predict outcomes in skin lymphoma patients.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

A woman with lupus and Kikuchi-Fujimoto disease improved with treatment.

Oral ulcers are common in SLE patients and often link to other symptoms.

A young girl developed unusually long eyelashes with a hair loss condition without other health issues or medication causes.

Tricholemmoma is linked to Cowden syndrome and can be benign or malignant.

Some leukemia treatments can cause skin reactions similar to keratosis pilaris.

Bullous pemphigoid can look like erythema multiforme, so awareness is needed for proper treatment.

The patient with EEC syndrome had scarring alopecia due to deep folliculitis, possibly linked to abnormal hair structure.

Stress may cause sudden hair whitening in children.

A 15-year-old with KID syndrome developed a rare skin condition called PEHFN.

The patient with lupus and Degos' disease showed significant improvement with treatment.

Hair thinning and loss in a girl with a rare metabolic disorder was linked to her condition.

Hair dysplasias involve various hair disorders causing fragility, breakage, and poor hair adhesion.

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

A unique type of lupus panniculitis causes reversible hair loss on the scalp in East Asians.

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

More skin lesions in lupus patients may indicate higher disease activity.

Lichen Planus is a less common condition affecting skin and mucous membranes, with various types and associated risk factors, challenging to diagnose, significantly impacts life quality, and may have a risk of cancerous changes in oral lesions.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

Dermatologists give better information on pathology forms, hypersensitivity vasculitis is a common skin issue, misdiagnoses can occur, and various skin conditions are linked to loss of elastin or genetic factors.

Previous alopecia areata treatments do not affect the long-term effectiveness of ritlecitinib.

An Australian with rare hair loss and eye conditions had a gene linked to both, not seen together before.

Pincer nails are rare in lupus patients and may be managed conservatively.

Hair-shaft abnormalities can indicate neurological disorders, some of which are treatable.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

The RAS pathway affects hair growth differently in CFCS and CS.

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

Focal palmoplantar callosities may help diagnose non-Herlitz junctional epidermolysis bullosa.