Search

everythinglearnresearchcommunity

for

Search:↓

The document concludes that an experimental drug may help wound healing in Epidermolysis Bullosa, links Hydroa vacciniforme to EBV, discusses diagnosing hair loss disorders, finds many children with eczema have allergies, reviews the safety of a skin medication in children, notes side effects of a Duchenne's treatment, and identifies a marker for pediatric mastocytosis.

Genetic mutations can affect female sexual development, requiring personalized medical care.

The newborn with Klippel-Trénaunay syndrome was healthy but needed regular check-ups for possible complications.

Alopecia areata in infants may be more common than previously thought.

Genetic testing can help diagnose skin conditions but needs more research for full effectiveness.

The document concludes that early and accurate diagnosis of hair loss on the top of the scalp in Black men is important to distinguish CCCA from other types of hair loss.

Androgenetic Alopecia (AGA) greatly lowers quality of life, causing stress and low self-esteem, with those seeking treatment experiencing more impairment.

Experts met to improve care for ichthyosis patients in Spain.

Two drugs, finasteride and minoxidil, are approved for hair loss treatment, but new therapies are being developed.

Abnormal gene expression related to keratin causes hair loss in certain mice.

The hair growth serum Trichosera® was effective in increasing hair regrowth and density and reducing hair fall without significant side effects.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

Some treatments for hereditary hair loss are effective but vary in results and side effects; new therapies show promise but need more research.

Trichoscopy helps accurately diagnose Netherton syndrome, often mistaken for atopic dermatitis.

Many men with androgenic alopecia also have dyslipidemia.

The term "Porokeratotic Adnexal Ostial Nevus" is suggested as a more appropriate name.

Cantú syndrome is caused by mutations in the ABCC9 gene.

Different fields of expertise must work together to better understand hair growth and create effective hair loss treatments.

Low levels of vitamin B12 and ferritin are linked to early hair graying.

Some natural ingredients like onion juice, rosemary oil, and pumpkin seed oil may help with hair growth and reducing hair loss.

A boy's hair that was frizzy and hard to comb returned to normal after 9 months, possibly due to genetic factors.

Lipedema is a painful fat disorder in women that's hard to treat, often worsens with hormonal changes, and requires symptom-focused therapies.

Hypothyroidism may cause certain types of hair loss.

The woman has a rare skin condition called follicular Dowling-Degos disease, which has limited treatment options.

Using stem cells from hair follicles to treat female hair loss is safe and effective after six months.

The young woman has a benign, hereditary skin condition with no signs of a more serious syndrome.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

A girl with a rare skin condition called Keratosis Follicularis Spinulosa Decalvans showed no significant improvement with treatment.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.