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Modern science supports the use of some Ayurvedic plants for health, as ancient practices suggested.

Frontal Fibrosing Alopecia in men is often missed and can come with symptoms like facial bumps and hair loss on eyebrows and limbs.

The conference presented findings on how vitamin D levels, genetic factors, and lifestyle choices like smoking and yoga affect various health conditions and diseases.

Eating barley for life may lead to healthier aging in mice.

Longer anogenital distance may indicate a higher chance of having polycystic ovary syndrome, and measuring this distance along with hormone levels could improve diagnosis.

Male pattern baldness is not a risk factor for heart disease based on cholesterol levels alone.

Many people in Saudi Arabia use vitamin D supplements, but few experience toxicity, showing the need for professional guidance when taking these supplements.

Alopecia areata, a common autoimmune hair loss condition, often runs in families.

Most patients with Porphyria Cutanea Tarda had skin blisters and were often affected by hepatitis C and alcohol abuse, with differences between familial and sporadic cases.

Some families have a genetic condition where they are born with irregular scalp defects.

Eruptive vellus hair cysts can run in families.

Familial factors affect hair loss types in Koreans, with M type in men, L type in women, and paternal factors influencing male hair loss more.

Treatment with dutasteride, minoxidil, and artificial hair transplantation improved appearance but caused folliculitis.

The conclusion is that hair loss from CCCA may be genetic and not solely caused by hair grooming practices.

Frontal fibrosing alopecia in families shows similar signs to individual cases and may have a genetic link.

A genetic marker linked to a type of hair loss was found in most patients studied.

A boy with a rare form of early puberty caused by a new gene mutation responded well to treatment aimed at reducing testosterone and preserving adult height.

Frontal fibrosing alopecia has occurred in two related male families.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

HIV-positive pregnant women are more likely to experience severe bleeding, and a pregnant woman with familial hypertriglyceridemia had a successful early delivery with special care.

Two young siblings experienced hair loss without hormone issues or other skin problems.

Familial frontal fibrosing alopecia is rare, mostly affects women, and often occurs between sisters or mother-daughter pairs.

A girl inherited excessive body hair from her mother and grandmother.

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

Premature hair graying in the face may be influenced by genetics and environment.

Two siblings were the first reported cases of inheriting both eye coloboma and loose anagen syndrome together.

A new genetic mutation in the TRPV3 gene causes Olmsted-like syndrome in a Mongolian family.

Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

Newborn acne may be linked to family history of high male hormone levels.

Cantú syndrome may be linked to pituitary adenomas.