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A young man had a rare case of hair cysts on his elbows, which was hard to diagnose and treat.

A 9-month-old baby had a rare, persistent ring-shaped hair loss condition.

A young girl developed serious bone inflammation in her skull after a skin graft, which is a rare but severe condition.

A 4-year-old girl had a rare hair disorder affecting only part of her scalp.

A young woman with a rare fungal infection showed significant improvement after treatment with antifungal medication.

A 70-year-old woman with a rare skin condition improved after treatment with topical steroids and acitretin.

Mother and son diagnosed with a rare genetic hair loss condition with no effective treatment.

A 46-year-old man showed symptoms of a rare condition usually seen in postmenopausal women, highlighting the need for dentist-dermatologist collaboration.

Minoxidil use was linked to a rare eye condition that improved after stopping the treatment.

Marie-Unna Hereditary Hypotrichosis is a rare genetic condition causing sparse hair growth, requiring specific recognition for proper care.

A woman with thymoma developed a rare chronic condition similar to graft versus host disease after surgery.

Popliteal Artery Entrapment Syndrome (PAES) is a rare but possible cause of leg pain during walking, even in untrained women.

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.