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A boy with a rare skin condition and kidney disease improved with cyclosporine after steroids failed, suggesting a new treatment approach.

One twin girl has Loose anagen syndrome with poorly anchored hair, diagnosed with a simple hair pull test, while her identical twin does not have the condition.

Treatment with vitamin A did not improve the child's skin condition.

A 21-year-old had a rare developmental anomaly with a misplaced sebaceous gland in a hair follicle.

A rare, harmless hair condition was found in an infant's eyebrow, needing no treatment.

A rare case of trichothiodystrophy was found with autism, seizures, and mental retardation.

Lhx2 is a crucial regulator of the Sonic Hedgehog signaling in early mouse retinal development.

Three siblings had both Vohwinkel's disease and congenital alopecia, with no effective treatment.

Unani medicine may help treat a rare, hard-to-treat hair loss pattern in children.

A 17-year-old girl and her brothers have a rare hair condition with long eyelashes, thick eyebrows, and easily pluckable hair.

Mutations in NIPAL4 cause skin issues by disrupting lipid layers, but some improvement is seen with topical treatment.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

Porokeratotic eccrine and hair follicle nevus is a very rare skin disorder possibly caused by a GJB2 gene mutation.

Lizard claws have hair-like keratins similar to those in mammals.

New genetic variants linked to inherited ichthyoses were identified, offering insights for potential gene therapy.

Systemic steroids effectively treated severe nail issues in a card illusionist with alopecia areata.

Schimmelpenning Syndrome requires careful evaluation and tailored treatment for skin, eye, and developmental issues.

A 10-month-old boy with a rare combination of genetic conditions has severe immune deficiency and treatment challenges.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

Early diagnosis and multidisciplinary care, including orthopedic surgery, can prevent long-term disability in IFAP syndrome.

Experts met to improve care for ichthyosis patients in Spain.

Laser treatments are the most effective for porokeratotic adnexal ostial nevus.

Early diagnosis and genetic evaluation of ADULT syndrome are crucial to reduce stress and medical costs.

Fox Fordyce disease might be more common in prepubertal girls than thought and can be managed with treatment.

Hair root analysis can effectively detect somatic mosaicism in double cortex syndrome.

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