Search

everythinglearnresearchcommunity

for

Search:↓

The document concludes that managing PCOS involves lifestyle changes, medication, and monitoring for associated health risks.

The document concludes that permanent hair loss conditions are complex, require early specific treatments, and "secondary permanent alopecias" might be a more accurate term than "secondary cicatricial alopecia."

The vitamin D receptor is crucial for bone health and affects various body systems, with mutations potentially leading to disease.

Hair loss can indicate underlying systemic diseases and addressing these can sometimes reverse the hair loss.

Fingerprints form uniquely before birth due to specific genetic pathways and local signals.

Eph/ephrin signaling is important for skin cell behavior and could be targeted to treat skin diseases.

Most hair loss in children is caused by a few common conditions, and it's important to diagnose these properly and support the child's mental health.

The guide helps doctors diagnose hair problems by suggesting a thorough patient history, physical exams, and various diagnostic tools.

The clinical signs of Adams-Oliver syndrome can vary greatly, even among family members.

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

PTHrP is important for bone formation and may be targeted for osteoporosis treatment and longevity therapies.

Congenital atrichia is a rare condition where children are born without hair, and treatment is often ineffective.

Fatty acid transport protein 4 is essential for skin and hair development.

The review suggests that other immune cells besides CD8+ T cells may contribute to alopecia areata and that targeting regulatory cell defects could improve treatment.

Some children are born with unusually short, fine hair because their hair growth phase is short, but this often gets better by itself during puberty.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

The document concludes that the girl's hairlessness is likely inherited from her parents.

A boy and his father with hereditary hypotrichosis simplex were treated for hair loss, but the treatment result is unknown.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

Alopecia areata is relatively common in children, has a variable course, and shows different responses to treatment; thyroid testing is recommended for those affected.

A woman with CHILD syndrome showed skin abnormalities, and the report suggests CHILD nevus and NEVIL might be the same condition, highlighting the need for diagnosis for genetic advice.

The research shows that a gene called Wnt3 affects hair growth and structure, causing short hair and balding when overactive.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

Too much Smad7 can cause serious changes in skin tissues, including problems with hair growth, thymus shrinkage, and eye development issues.

Acquired Progressive Kinking of Hair is likely an early sign of male pattern baldness.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

Recent findings suggest that genetic factors, immune system issues, and skin cell defects might contribute to the development of hidradenitis suppurativa.

MOF controls key genes for skin development by regulating mitochondrial and ciliary functions.

People distressed by minor skin changes should consult dermatologists with cosmetic expertise, and a public Cosmetic Dermatology Service with mental health support is recommended.

Combining genetic and physical trait analysis improves diagnosis accuracy for monogenic diabetes.