Search

everythingexperts & clinicslearnresearchcommunity

for

Search:↓

T cell subsets are crucial in kidney cancer, and a new model predicts patient outcomes using key genes.

The research mapped diverse cell types in mouse lacrimal glands, aiding understanding of gland biology and diseases.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

Ovarian hyperthecosis can cause polycythemia, and surgery can normalize symptoms.

New technologies show potential for better understanding and treating skin conditions with abnormal mucin, but more research is needed for clinical use.

Skin tumors with CYLD cutaneous syndrome show more NF-κB activity and less organized collagen.

Leukemia can sometimes appear as unusual skin issues in children.

Mutations in the DSG4 gene cause a severe form of brittle hair and skin issues.

SLE is likely one disease with various symptoms, not multiple distinct diseases.

Azithromycin can rarely cause a severe drop in white blood cells.

Dual TCR Treg cells are common in mouse tissues and vary by location.

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

A common mutation in the hHb6 gene is linked to monilethrix, but other factors may also play a role.

PAON shows skin patterns due to genetic mosaicism.

A man with Cronkhite-Canada syndrome had all 20 nails detach but improved with treatment.

A 12-year-old girl was diagnosed with monilethrix, a genetic condition causing fragile, beaded hair that breaks easily, with no effective treatment available.

A new mutation, Glu402Lys, in hair keratin is linked to variable symptoms of monilethrix.

A man with rare skin changes on his fingers was diagnosed with multiple myeloma-linked amyloidosis.

Anti-MND antibodies are present in various diseases, not just PBC, and their levels don't correlate with disease activity or skin symptoms.

Cyclophosphamide often causes gastrointestinal issues, hair loss, and low blood cell counts in Chinese patients with autoimmune diseases.

Mast cells may significantly contribute to central centrifugal cicatricial alopecia.

A man with a skin nodule was diagnosed with a rare skin condition called cutaneous focal mucinosis, which can be confused with other skin cancers.

Monilethrix is a genetic hair disorder affecting hair shape, seen in two brothers.

Multiple perifollicular fibromas may actually be unrecognized cases of Birt-Hogg-Dubé syndrome.

Monilethrix causes different levels of hair loss in family members.

The man's diarrhea was caused by a rare disorder called Cronkhite-Canada syndrome, which improved with specific medications.

Primary mitochondrial cytopathies often cause skin, endocrine, vision, and blood issues, needing careful diagnosis.

Monocyte-derived dendritic cells play a key role in UVB-induced skin sensitivity and inflammation.

A man's skin condition was misdiagnosed and later identified as a rare type of skin cancer, which did not improve with treatment.