Search

everythinglearnresearchcommunity

for

Search:↓

Baricitinib reduces inflammation and improves cell health in premature aging cells.

Rapp-Hodgkin syndrome, AEC, and EEC are different expressions of the same genetic disorder caused by TP63 gene mutations.

Erythromelanosis follicularis faciei can also affect women, though it's rare.

New treatments for ichthyosis, like protein replacement and gene therapy, show promise and may become standard care.

The fuzzy gene is crucial for controlling hair growth cycles.

The document talks about hard-to-treat and rare acne types, their connection with other health issues, the importance of correct diagnosis, and the challenges in managing them.

A baby with a rare metabolic disorder developed a rash not cured by zinc alone, likely due to both zinc and amino acid deficiencies.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

A rare gene mutation causes skin fragility and itching without affecting hair or nails.

The document reports a unique case of woolly hair with a combination of conditions not previously seen together.

Advances in genetics may lead to targeted treatments for hair disorders.

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.

Knocking out certain genes in mice helps understand skin and hair growth problems.

Leptin-deficient mice, used as a model for Type 2 Diabetes, have delayed wound healing due to impaired contraction and other dysfunctional cellular responses.

Narrowband UVB therapy significantly improved a child's rare skin condition.

Laser hair removal is effective for hirsutism when combined with treatment for the underlying causes.

Sudden, unusual hair loss may indicate serious underlying health issues.

Foam corticosteroid covers as well as traditional forms.

A woman with lupus had muscle weakness due to kidney issues and was successfully treated with medication.

"D-CHRAMPS syndrome" is a newly identified condition with multiple severe symptoms.

In India, most patients with type 1 autoimmune polyglandular failure show symptoms in a specific order, starting with parathyroid gland issues, then yeast infections, and finally adrenal gland failure.

Imaging helps detect adrenal gland issues and monitor treatment in congenital adrenal hyperplasia, and can identify tumors affecting fertility.

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

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

Glucocorticoids for progressive muscular dystrophy in children don't improve muscle strength or function but do increase certain side effects.

The girl has both monilethrix and Type 1 diabetes, but no link between the two conditions is known.

A 17-year-old in Saudi Arabia was diagnosed with a rare skin condition causing red-brown facial patches.