Search

everythinglearnresearchcommunity

for

Search:↓

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

An 11-year-old girl with Trichotillomania developed a large hairball in her stomach, treated with medication, therapy, and family education.

Tislelizumab can cause cutaneous lupus erythematosus.

Two siblings were diagnosed with Trichothiodystrophy, identified by brittle hair and low sulfur content.

Recognizing minor skin lesions can help identify serious cancer syndromes.

Antituberculosis drugs can cause severe skin reactions, requiring careful diagnosis and treatment.

Temporal triangular alopecia usually starts in early childhood and treatment with Minoxidil has limited effectiveness.

Trichoscopy is reliable for diagnosing Temporal Triangular Alopecia and can prevent unnecessary biopsies and wrong treatments.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

Cantú syndrome may be linked to pituitary adenomas.

Focal palmoplantar callosities may help diagnose non-Herlitz junctional epidermolysis bullosa.

HTLV-1-associated lichenoid dermatitis (HALD) is linked to an immune response against HTLV-1-infected cells.

Genetic testing confirmed a rare disorder causing hair loss and vision problems in a Saudi family, stressing its importance for diagnosis and counseling.

Trichoscopic examination is crucial for diagnosing congenital triangular alopecia.

Tofacitinib may cause nerve damage in the brain, so monitor for neurological symptoms.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Tofacitinib helps improve skin conditions in people with Down syndrome, especially alopecia areata.

Hair tourniquet syndrome is a rare condition where hair wraps around an infant's body part, needing quick removal to prevent damage.

Alopecia triangular temporal is a rare condition with unclear causes and treatment, but trichoscopy helps in diagnosis.

Hair-thread Tourniquet Syndrome, where hair or thread tightly wraps around a body part, is not rare and requires early detection to prevent serious damage.

Hair tourniquet syndrome in infants can be treated successfully with immediate hair removal.

A patient with Satoyoshi syndrome improved with a treatment combining several medications, including carbamazepine and methotrexate.

Early diagnosis and treatment with corticosteroids can improve outcomes in Cronkhite–Canada syndrome.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

A young tapir with a rare skin condition improved after treatment with wound cleaning, cream, and oral medication.

Tigers had a skin condition causing hair loss and inflammation, but the cause is unknown and treatment didn't work.

Satoyoshi Syndrome is hard to diagnose and treat due to its rarity and complex symptoms.

A new genetic mutation in the TRPV3 gene causes Olmsted-like syndrome in a Mongolian family.

The document suggests a rare skin condition might be caused by a genetic phenomenon.