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Post-steroid panniculitis is now rare because doctors taper steroids more carefully.

PRP therapy and hair transplants can cause rare but treatable scalp hematomas.

Steroid use can cause a rare eye condition called central serous retinopathy, which can lead to permanent vision damage.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

A 19-month-old Saudi girl had a rare skin condition with no other defects, and her family was unaffected.

Primary cicatricial alopecia, a rare disorder causing permanent hair loss, is hard to diagnose and treat, with treatments like anti-inflammatory drugs and steroids offering varied results and no guaranteed cure. Psychological support for patients is important, and future research should aim to identify causes of the condition.

FGF13 gene changes cause excessive hair growth in a rare condition.

Hair thinning and loss in a girl with a rare metabolic disorder was linked to her condition.

New hair and skin changes were found in a rare case of syphilis-related hair loss.

A teenage girl with high androgen levels and PCOS developed a rare liver tumor, suggesting a possible link between high androgens and the tumor's growth.

Topical contact sensitizers can treat certain skin conditions but are rarely used in the U.K.

HPV vaccines are generally safe but need further investigation for rare side effects.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

The study found unique skin changes in a rare type of alopecia linked to a skin condition called linear morphea.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

Early diagnosis and aggressive treatment are key for managing rare scalp disorders that cause permanent hair loss.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

A 15-year-old with KID syndrome developed a rare skin condition called PEHFN.

Some patients with a type of skin lymphoma can experience a rare, non-scarring hair loss that looks like another hair loss condition but has distinct features.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

Minoxidil can cause severe skin reactions like Stevens-Johnson syndrome in rare cases.

A woman with long-term scalp psoriasis developed rare scarring hair loss that didn't fully respond to treatments.

Researchers found a gene mutation responsible for a rare hair loss condition.

A woman with acromegaloidism and normal growth hormone levels had a rare X-Tetrasomy, suggesting a need to study X-chromosome genes for their role in growth and facial development.

Steroid treatment greatly improved the symptoms of a boy with a rare disorder called Satoyoshi syndrome.

An 18-year-old girl was diagnosed with a rare hereditary hair loss condition, despite no family history.

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

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Narrowband UVB therapy significantly improved a child's rare skin condition.

A dog in Germany was successfully treated for a rare bacterial infection without spreading it to humans.