Search

everythinglearnresearchcommunity

for

Search:↓

Björnstad syndrome can cause hair loss similar to androgenetic alopecia, and treatment with baricitinib and minoxidil may help.

A 15-year-old girl with hypothyroidism had excess hair and skin issues due to blocked hair follicles.

A rare combination of halo nevi, nonsegmental vitiligo, and early gray hair can occur together.

Autoimmune Polyendocrine Syndromes involve specific combinations of autoimmune diseases.

The early genes of a specific virus can cause abnormal skin cell growth and hair follicle changes.

Mutations in the ST14 gene cause skin and hair issues by disrupting important protein processing.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

A teenager had both alopecia areata and vitiligo, which are rare to occur together.

A young boy with Netherton syndrome improved significantly using IVIG, dupilumab, and dietary changes.

Hutchinson-Gilford Progeria Syndrome causes rapid aging due to a gene mutation, with no cure yet, but research may lead to better treatments.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

The hair disorder was caused by abnormal protein formation, making hair easily damaged.

Catatonia can be a rare sign of lupus, needing careful diagnosis and treatment.

Thymoma may link myasthenia gravis, nail dystrophy, and alopecia areata.

Two cases of hairy elbows syndrome were described, with normal skin texture and symmetrical hair growth.

The patient likely has Chrousos syndrome, a rare condition causing insensitivity to glucocorticoids, requiring high-dose dexamethasone treatment.

Trichoscopy is useful for diagnosing Netherton syndrome in children with skin issues.

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

KID syndrome should be reclassified as an ectodermal dysplasia.

Long eyelashes in a patient were an unusual sign of systemic lupus erythematosus.

Thorough hair examination is crucial for accurate diagnosis and treatment.

A six-year-old boy with excessive hair growth and other symptoms may have a genetic link on chromosome 17q, requiring regular medical follow-ups.

The girl's condition improved with treatment, showing no new autoimmune diseases and hair regrowth.

Trichotillomania is a complex condition involving compulsive hair pulling that causes distress and hair loss.

The conclusion is that the variation in hair thinness in patients is mostly due to the amount of underdeveloped hairs, and treatments that thicken fine hairs might work for those with mild to severe conditions.

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

The woman's facial symptoms are best explained by primary Sjögren’s Syndrome.

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