Search

everythinglearnresearchcommunity

for

Search:↓

The enzyme steroid sulfatase is linked to breast cancer and other conditions, and inhibitors are being developed for treatment.

Congenital Adrenal Hyperplasia is a rare inherited disease causing hormone imbalances, affecting growth, fertility, and heart health, diagnosed through blood tests and treated with medication and lifestyle changes.

Combining minoxidil and plant extracts improved hair growth in a boy with a rare genetic disorder.

Leptin affects skin and hair health and may worsen some skin conditions, but more research is needed to understand its full impact.

EVG staining is a valuable, simple, and cost-effective method for diagnosing various skin conditions in dermatopathology.

Assessing newborn scalp hair can reveal important health information.

Pattern baldness is likely caused by a dominant gene influenced by testosterone levels, making it more common in men.

The conclusion is that adult males with muscle weakness and hormonal imbalances should be tested for Kennedy's disease.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

Taking riboflavin and eating less lysine can help some people with a specific genetic disorder avoid brain damage.

Creating stronger blockers for skin enzymes might lead to better treatment for conditions like acne and excessive hair growth.

The document concludes that understanding hair biology and recognizing hair conditions are crucial for managing and treating hair loss in children.

Childhood ptosis can vary from a minor cosmetic issue to a serious condition and may signal other health problems.

Melanoma risk tools need improvement, certain gene mutations cause skin diseases and could be treated by targeting those mutations, skin wrinkling may relate to lung aging due to genetic factors, and oxidative stress affects hair loss but can be reduced in low oxygen.

New genes linked to ichthyosis were found, but there's still no cure; treatment options are improving.

Researchers found a new mutation causing total hair loss from birth.

A man with itchy skin lesions and weight loss was diagnosed with a rare skin condition linked to a pancreatic tumor.

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

K_ATP channel gene mutations are linked to heart diseases, but more research is needed to understand the connection and treatment potential.

Different hair and scalp disorders cause hair loss or excess hair growth, with various treatments available depending on the specific condition.

Diabetes often causes various skin problems and complications.

Hair steroid measurement is an effective method to diagnose and monitor CAH in developing countries.

The L412F variant of TLR3 is linked to skin infections, more viral infections, and autoimmune issues.

The study found no common cause for a girl's crystalline cataract and uncombable hair, suggesting their co-occurrence might be coincidental.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

Premature aging increases the risk of immune problems and autoimmune diseases.

Men's sensitivity to male hormones might affect how severe COVID-19 gets for them.

The research found that a specific gene mutation causes fewer hair follicles and disrupted hair growth cycles, leading to thin and short hair in people with Hypotrichosis with Juvenile Macular Dystrophy.

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