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Clouston syndrome is inherited in an autosomal dominant pattern and caused by a specific gene mutation, with no current treatment available.

GLPLS is a rare skin condition with specific hair loss and skin symptoms.

A person with Turner Syndrome showed severe schizophrenia that didn't respond to treatment and had brain shrinkage.

Enteral supplements can improve symptoms of Cronkhite-Canada syndrome.

A 20-year-old woman with a rare form of Turner syndrome showed improvement with hormonal therapy and needs comprehensive care.

Early recognition and management of gastrointestinal tuberculosis in lupus patients are crucial to prevent complications.

Gomez–Lopez–Hernandez syndrome can cause focal hair loss and developmental delays but some children can still function well and excel in school and sports.

A boy with toxic shock syndrome had severe heart rhythm problems but recovered with treatment.

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

The research suggests that Tourette syndrome is linked to both brain signaling and immune system pathways.

Leflunomide successfully treated a rare skin condition in a liver transplant patient.

Loose anagen hair syndrome causes easily pulled, thin hair in kids but is harmless and temporary.

Patients with alopecia areata should be checked for muscle spasms, diarrhea, and ANA to avoid missing Satoyoshi syndrome.

Late dumping syndrome after fundoplication can be diagnosed with an oral glucose tolerance test and managed with diet changes.

Narrowband-UVB phototherapy successfully treated a rare case of Graham Little-Piccardi-Lassueur syndrome.

Tacrolimus and corticosteroids can improve symptoms of Satoyoshi syndrome.

Steroid pulse therapy improved symptoms in a man with Satoyoshi syndrome.

Rothmund-Thomson syndrome causes skin changes, hair loss, and slightly high lysine and cystine in urine.

Small bowel lesions in Cronkhite-Canada syndrome persist despite steroid treatment.

A rare skin condition was confirmed to be associated with a specific virus in a young girl.

A child has a rare hair and skin disorder due to specific gene variants, suggesting broader genetic testing is needed.

The document reports three sisters with Woodhouse-Sakati syndrome showing typical symptoms and unusual gynecological anomalies.

A Laotian man with unusual skin changes and multiple growths in his gut was diagnosed with Cronkhite-Canada Syndrome and improved with nutritional and immune-based treatments.

A 14-year-old girl with no menstrual period was diagnosed with Swyer Syndrome and treated for a related cancer risk.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

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

Cronkhite-Canada syndrome can cause multiple gastrointestinal polyps and various physical symptoms.

A child with Olmsted syndrome showed mild improvement in hair and skin issues with treatment.

Botulinum toxin injections greatly reduced pain in Parry-Romberg syndrome.