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Patients with central centrifugal cicatricial alopecia may have a higher risk of breast and colorectal cancer.

A woman's new seizures were caused by a brain tumor likely linked to her past cancer treatment, and choosing safe seizure medications is important for women who can have children.

CTHRC1 is essential for healing and preventing heart rupture after a heart attack.

A patient with Rothmund-Thomson syndrome showed skin changes, hair loss, and dental defects but no cataracts or skeletal issues.

Pyoderma gangrenosum can occur in rheumatoid arthritis patients and may be mistaken for vasculitis.

The boy's symptoms improved with vitamin C treatment, highlighting the need to consider scurvy in kids with unusual diets.

Enzyme replacement therapy may help alleviate symptoms in complex cases like this.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Anti-Ku-positive patients often have muscle weakness and autophagy plays a key role in their condition.

A 12-year-old boy had severe shingles and skin damage after a stem-cell transplant.

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.

Tislelizumab can cause cutaneous lupus erythematosus.

People with celiac disease have a higher risk of developing alopecia areata.

The twins' condition is unique and doesn't match any known syndromes.

A new type of hereditary hair loss in a Chinese family is linked to chromosome 2p25.1–2p23.2.

The document concludes that doctors should recognize congenital triangular alopecia to avoid unnecessary treatments, as it does not respond to steroids like alopecia areata does.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

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

KLHL24-mutant stem cells help understand skin and heart disease.

Keratin 17 gene mutations cause both steatocystoma multiplex and pachyonychia congenita type 2.

Hair changes could indicate neurological diseases and help monitor treatment.

The boy's symptoms suggest a possible new medical condition.

The study concluded that careful examination is key to differentiate between lipidized fibrous histiocytoma and juvenile xanthogranuloma.

Long-COVID can cause lasting symptoms, but treatment with Erbisol drugs may help.

A woman with CCCA has hair loss due to factors like straighteners and tight hairstyles, and treatments include steroids and avoiding certain hair products.

Most Recessive Dystrophic Epidermolysis Bullosa patients with a specific mutation likely have Sephardic ancestry from about 500 years ago.

A rare skin condition in a baby showed unusual fat and hair follicle changes.

A rare skin condition usually found near the eyes was found on a farmer's scalp.

Porokeratotic eccrine and hair follicle nevus is a very rare skin disorder possibly caused by a GJB2 gene mutation.