Search

everythinglearnresearchcommunity

for

Search:↓

Researchers created human cells that can turn into sebocytes, which may help study and treat skin conditions like acne.

Certain miRNAs might be involved in a hair loss condition called frontal fibrosing alopecia and could possibly help in its diagnosis.

HIF-1A may aid hair growth, Backhousia citriodora improves skin, autologous cells stabilize hair loss, infrared thermography assesses alopecia, and a new treatment preserves hair.

The new scalp treatment preserves hair color, reduces hair loss, and maintains hair strength.

Stabilizing HIF-1A in hair follicles may reduce oxidative stress and promote hair growth by increasing glycolysis.

Dutasteride improved hair density and thickness in men not helped by finasteride, with minimal side effects.

Some men don't respond to common hair loss treatments, but a new inhibitor, FOL-005, shows promise for targeting unwanted hair growth.

Injections of special skin cells showed potential in treating hair loss, with some participants experiencing increased hair density.

Finasteride helps female-pattern hair loss.

Higher BMI, IGF-1, and DHEAS levels are linked to advanced bone age in young Chinese girls with early breast development.

A 2-year-old boy with a rare brain malformation may have Gomez–López-Hernández syndrome.

A 15-year-old girl with no menstrual period was diagnosed with a genetic condition that makes her body unable to respond to male hormones, leading to female characteristics despite having male genetic makeup.

Most skin conditions in Down syndrome are benign and involve dry or thickened skin.

Conditions affecting sex development show that sexual diversity is a natural part of human variation.

Get head MRI for babies with achondroplasia early, use free immunoglobulin light chains to detect certain neurodevelopmental disorders, and video calls work for speech therapy in patients with facial anomalies.

Ayme-Gripp Syndrome was confirmed in a woman through genetic testing, highlighting the need to consider rare genetic conditions in diagnoses.

A 15-year-old girl with missed periods was diagnosed with a pituitary disorder and treated with hormones and steroids.

Dexamethasone effectively normalizes elevated steroid levels in girls with premature adrenarche.

Two brothers from Bangladesh were diagnosed with X-linked adrenoleukodystrophy, showing neurological and adrenal symptoms.

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.

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

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

Excess maternal androgens can cause heart problems in offspring.

A newborn girl has a rare skin condition with two ulcers on her buttock that are healing on their own.

The condition is likely inherited in an autosomal-dominant pattern.

A 12-year-old girl's hair loss was linked to a rare genetic condition called ALX4-related frontonasal dysplasia.

A 36-year-old person with a female appearance but male chromosomes was diagnosed with a rare enzyme deficiency affecting sexual development.