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KFSD is a rare condition causing scarring hair loss, with no effective treatment known at the time of the report.

Somatic BHD mutations are rare in Japanese renal tumors.

Idiopathic hypoparathyroidism is rare and can be managed with dihydrotachysterol.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

NISCH syndrome is a rare genetic disorder affecting skin and liver, with variable symptoms and limited treatment options.

Nevus comedonicus is a rare skin condition with grouped open pores, sometimes linked to other body issues.

A hair strand caused a rare case of limb strangulation in a teenage girl with autism, and the condition is not always linked to child abuse.

Some psychotropic medications can rarely cause hair loss, and stopping these drugs usually reverses the condition.

Some medications can cause rare hair color changes, and reporting these side effects is important for patient quality of life.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

Acrodermatitis enteropathica is a rare inherited disorder causing skin issues, diarrhea, and hair loss.

Pediatric alopecia areata is rare, affecting more girls than boys, and peaks at ages 9-12.

Psoriasis can cause rare vulval scarring.

New techniques helped identify rare wool proteins by reducing dominant ones.

Dupilumab can cause rare side effects like a rash on the face and neck.

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

Beta-blockers can cause rare skin side-effects, which usually improve after stopping the medication.

A 6-year-old girl was diagnosed with a rare hair disorder and started treatment with topical minoxidil.

Trichodysplasia spinulosa is a rare skin disease in immunocompromised patients caused by a specific virus targeting hair follicle cells.

A child's rare skin disease was triggered by chickenpox.

Pseudopelade is a rare inherited hair loss condition with a genetic cause.

Clouston Syndrome can be linked to rare sweat gland tumors.

Two patients with a rare scalp fungus in Poland were successfully treated with griseofulvin and ciclopirox.

A baby with a rare metabolic disorder developed a rash not cured by zinc alone, likely due to both zinc and amino acid deficiencies.

A woman's rare adrenal tumor caused high testosterone and cortisol levels, which normalized after the tumor was removed.

Tinea capitis is rare in healthy adults but should be considered in scalp issues.

Demodex mites rarely cause scalp infections leading to hair loss, but when they do, treatment is effective.

Zouboulis syndrome is a rare condition that helps diagnose monosomy 18p early.

rPanglaoDB helps study rare cell types by merging RNA data, showing fibrocytes aid in healing.

Viral reactivation is rare at the time of DRESS diagnosis in the U.S.