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A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Taste disorders in Cronkhite-Canada syndrome are severe in the front of the tongue but improve with treatment.

A Japanese patient with a rare genetic disorder had a less severe case than others, suggesting other factors may affect symptoms.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

The document describes a rare case of IFAP syndrome, a genetic condition with symptoms of hair loss, light sensitivity, and scaly skin.

Trichoepithelioma and desmoplastic trichoepithelioma have distinct features that can be identified using reflectance confocal microscopy.

Giant solitary trichoepithelioma is a rare, usually non-cancerous hair follicle tumor that can sometimes turn into skin cancer.

An 11-year-old girl with hair thinning was diagnosed with monilethrix and early androgenetic alopecia.

Sporadic trichoblastic neoplasms generally don't recur or spread, with one case showing a specific genetic fusion.

The condition is harmless, doesn't worsen, and needs no invasive treatment.

Loose anagen hair syndrome in children often resolves on its own.

Ossification in trichilemmal cysts is more common than previously believed.

The review found that individualized treatment and teamwork are important for trichotillomania, and patients who followed through with treatment often improved.

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

Iron deficiency anemia can cause hair breakage.

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

Immunohistochemistry helps accurately identify and differentiate malignant trichilemmoma.

Some people with schwannomatosis have a new type of mutation in the LZTR1 gene.

A 5-year-old girl with a rare genetic disorder, lipoid proteinosis, showed reduced new lesions but persistent scars after avoiding skin trauma.

The boy likely has a fungal infection causing hair loss.

Recognizing eyebrow hair loss linked to a rare skin condition is crucial for proper treatment.

Women of reproductive age with polycystic ovary syndrome often experience hair loss.

Treating scalp issues in hair-pulling disorder helps hair regrow and reduces itch.

A rare genetic mutation causes severe immune issues, hair loss, and nail problems.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

Hairy elbows may be linked to short stature, but the exact cause is unclear.

Thyrotropin-releasing hormone may help control skin and hair growth and could aid in treating related disorders.

One twin girl has Loose anagen syndrome with poorly anchored hair, diagnosed with a simple hair pull test, while her identical twin does not have the condition.