Search

everythinglearnresearchcommunity

for

Search:↓

A specific group of early-stage melanocytes is reduced in vitiligo-affected skin, which may explain treatment resistance.

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

A man had two rare autoimmune diseases that might be connected.

A boy with chromosome 13q deletion syndrome developed eye cancer, a woman with breast cancer lost vision due to a rare side-effect of her treatment, a man's vision worsened after using a hair loss drug, and two rare disorders were discussed. Optical Coherence Tomography is useful for diagnosing and monitoring these conditions.

Alopecia in these mice is caused by defective hair cycle communication due to missing vitamin D receptor function, not vitamin D levels.

Children with Parry Romberg Syndrome had successful facial fat-grafting surgeries after disease stabilization with no complications.

Topical DPCP is somewhat effective for hair loss in alopecia areata, but more research is needed.

First Korean case of Cronkhite-Canada syndrome with colon cancer and serrated adenoma.

Skin side effects from CDK4/6 inhibitors in breast cancer patients are generally mild and treatable, allowing most patients to continue treatment.

DPCP can help regrow hair in some people with severe alopecia.

Two transplant patients on cyclosporine unexpectedly developed hair loss.

The junction of the inner and outer prepuce with good blood flow is best for vascular pedicle flaps.

A new genetic variant in the EEF2K gene may contribute to polycystic ovary syndrome.

An 80-year-old woman with Cronkhite-Canada syndrome had multiple polyps and symptoms like diarrhea, hair loss, nail issues, and dark skin.

The girl's symptoms suggest a complex condition that's hard to diagnose despite normal test results.

Iron deficiency anemia may contribute to hair loss in women with Telogen effluvium.

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

Low androgen levels can still cause female pattern hair loss.

CTP-543 effectively promotes hair regrowth in adults with moderate to severe alopecia areata.

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

Yorkshire Terriers with Colour Dilution Alopecia have reduced melanin and hair structure issues.

PCOS affects 11% of women, highlighting the need for standardized diagnosis.

Trichodysplasia spinulosa is a rare skin disease in immunocompromised patients caused by a specific virus targeting hair follicle cells.

Deleting part of a gene in mice causes wavy hair and high pup loss.

In India, most patients with type 1 autoimmune polyglandular failure show symptoms in a specific order, starting with parathyroid gland issues, then yeast infections, and finally adrenal gland failure.

A rare skin condition in a 17-year-old was diagnosed late, stressing the need for careful evaluation and genetic testing.

A young woman's Cronkhite-Canada syndrome improved on its own after she gave birth.

The letter suggests that the study's comparison group might have affected the results and calls for larger, more detailed future research.

Psoriasis may be chronic because it lacks certain immune system controls that prevent overreaction.

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.