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The hydrogel helps reduce scarring and improve wound healing by releasing salvianolic acid B in acidic conditions.

A genetic variant in the KRT71 gene may cause loose anagen hair and wooly hair, and symptoms might improve with age.

CAH is a genetic disorder affecting cortisol production and causing hormonal imbalances, with treatment and diagnosis varying by form and symptoms.

The ZIP13 variant is linked to abnormal hair quality.

A boy with a rare birthmark called verrucous hemangioma needed careful timing for surgery due to its size and depth.

Skin organoids with NCSTN mutation show changes in hair follicle development and higher inflammation, key features of Hidradenitis Suppurativa.

A girl with hereditary chorea, likely Huntington's disease, had her condition worsened by lupus.

3D ultrasound can detect hair follicle changes and disease phases in alopecia areata.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

Mice without the enzyme HSD17B3 still produce normal testosterone, suggesting they have different ways to make it compared to humans.

Early recognition and treatment of VATS in transplant patients improve outcomes.

A child with a rare type of rickets showed some improvement with high doses of vitamin D, but such conditions often respond poorly to treatment.

A boy with severe Vitamin D-resistant rickets did not respond to treatment and lacked a common symptom, suggesting a need for alternative treatments.

A new mouse mutation causes skin and hair defects due to a gene change.

New SRD5A2 variants may disrupt protein function, aiding diagnosis and treatment of related disorders.

Early recognition and treatment of hidradenitis suppurativa in children are crucial to prevent complications.

Two sisters with Netherton's syndrome had skin and hair issues, needing special diet and ointments.

CYP11A1 is crucial for skin health and disease by producing important steroids.

Routine genetic testing is crucial for early diagnosis and better management of Turner’s syndrome with 21-hydroxylase deficiency.

Suppressing the HGPS mutation may improve symptoms and suggest reversibility.

Hair follicle stem cells can help treat eye surface issues by becoming corneal cells.

A 9-year-old Hispanic girl has Uncombable Hair Syndrome, which may improve with age and biotin treatment.

A new gene mutation linked to KID syndrome was found, expanding genetic knowledge.

Two siblings have a rare hair condition caused by a new genetic variant.

Hirsute women have lower type 2 17β-HSD enzyme levels, which improve with treatment.

A 4-year-old boy with a rare type of rickets and hair loss improved in bone health but not hair growth after vitamin D and calcium treatment.

Children with lower inhibitory control experience more stress when starting third grade.

New genes and pathways are important for testosterone production and male sexual development.

Lower 2D:4D finger ratios in HS patients suggest prenatal hormone influence on the disease.