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The gene for Clouston syndrome in a large Indian family is located in the 13q11-q12.1 region.

Hand-foot-mouth disease may cause nail loss in children.

Rhupus is a complex syndrome that combines rheumatoid arthritis and lupus, making diagnosis challenging.

Hair shaft changes may be linked to CCCA, but their role is unclear.

TRH stimulates human hair growth and extends the hair growth phase.

Thorough hair examination is crucial for accurate diagnosis and treatment.

Using tretinoin cream on the skin can get rid of hair plugs caused by Trichostasis spinulosa.

The TRPV3 channel structure changes linked to severe itch and hyperkeratosis were identified using cryo-EM.

The study concludes that Twenty-nail dystrophy is more common in boys among children and in women among adults, with varying response to treatment.

Oral isotretinoin temporarily improved skin symptoms in a child with IFAP syndrome.

A rare foot cyst was successfully diagnosed and removed without cancer.

Hair transplant complications were likely due to deep graft placement and rough handling.

A miner developed extra shoulder hair due to long-term work pressure and inflammation.

Long eyelashes in a patient were an unusual sign of systemic lupus erythematosus.

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

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

Trichilemmal carcinoma is rare, usually benign after removal, but needs close follow-up due to recurrence risks.

Understanding genes and mutations can lead to new treatments for hair loss disorders.

Age and diabetes are linked to larger trichilemmal cysts, while hypertension is linked to smaller ones.

Trichoscopy helps diagnose and assess the severity of Frontal Fibrosing Alopecia.

The document concludes that understanding hair structure is key to diagnosing hair abnormalities and recommends gentle hair care for management.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

The pseudo 'fringe sign' can also appear in frontal fibrosing alopecia, not just in traction alopecia, showing that this condition may be more common than thought.

A rare skin infection in a 10-year-old kidney transplant patient was successfully managed by adjusting medication.

More children are showing signs of hair-pulling disorders during the COVID-19 pandemic due to stress and lack of social interaction.

Trichoscopy is highly effective for diagnosing scalp disorders and should be used more in dermatology.

New genetic mutations linked to rare skin disorders were found in three newborns.

A baby's toe was saved from serious damage by quickly removing a hair wrapped tightly around it.

Uncombable hair is inherited dominantly with complete penetrance.