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Posterior column injuries are common in tibial plateau fractures, and CT imaging is crucial for accurate treatment planning.

Kerion cases had longer disease duration but responded well to antifungal treatments.

Scalp flaps are stiffer than skin from other body areas, which helps in planning reconstructive and cosmetic head surgeries.

Giant axonal neuropathy changes the structure of keratin in human hair, making it stiffer and stronger.

The curly mutation in SELH/Bc mice affects hair and may help study human genetic disorders.

Most patients with cutaneous dermatomyositis either improved or remained stable over 3.5 years.

Olmsted syndrome can be inherited as an autosomal recessive trait due to a rare TRPV3 gene mutation.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in Tourette syndrome patients.

Pili annulati is caused by a protein metabolism disorder affecting hair structure.

Burn reconstruction is crucial for improving long-term outcomes for burn survivors.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

Mechanical trauma like towel drying can cause knotted hair even in straight hair.

Keratosis Pilaris Atrophicans causes skin scarring and might be treated with a new synthetic retinoid.

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

Early recognition and tailored treatment are crucial for managing overlapping systemic lupus erythematosus and systemic sclerosis.

Uncombable hair syndrome causes dry, frizzy hair that can't be combed flat, seen in a young child.

A child with skin and heart issues had rare genetic mutations affecting skin and heart cell cohesion.

A 12-year-old girl in Saudi Arabia with Focal dermal hypoplasia showed skin and dental symptoms, highlighting the condition's variability and the need for personalized treatment.

Progerin affects cell shape but not hair or skin in mice.

FOXN1 mutations can cause varying immune and physical issues, with severity influenced by gene activity and possibly other factors.

Most patients with dermatomyositis had skin rash, itching, and muscle weakness, treated mainly with prednisolone and hydroxychloroquine.

A person was born with both a rare hairless condition and a type of birthmark, which is an uncommon combination.

Congenital atrichia with papular lesions causes permanent hair loss and skin bumps due to a gene mutation.

A brain injury can lead to compulsive hair-pulling and psychosis-like symptoms, needing comprehensive treatment.

Monilethrix is a rare, inherited condition causing fragile hair and hair loss, with no cure but some treatments may help.

Using a method of stretching skin multiple times can help cover large bald spots on the scalp, but it takes a long time and isn't good for kids.

Keratosis pilaris is a common skin condition where hair follicles get clogged with keratin, mostly on the arms and thighs.

The woman was diagnosed with lichen sclerosus, a rare skin condition, after initial misdiagnosis and ineffective treatments.

Mutations in the FOXN1 gene cause severe immune issues but don't affect hair and nails.