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A man with myotonic dystrophy type 1 had 28 skin cancers, suggesting a link between the disease and skin cancer, emphasizing the need for sun protection and regular skin checks.

Dupilumab helped improve skin and prevent new lesions in a child with a rare immune disorder and severe eczema.

New therapies are being developed that target integrin pathways to treat various diseases.

A new gene mutation may allow some piebaldism patients to regain skin color in white patches.

The lotion and shampoo effectively treated scalp seborrheic dermatitis.

Mutations in Gasdermin A3 cause skin inflammation and hair loss by disrupting mitochondria.

A 2-year-old boy had no hair and unusual organ placement, and it's unclear if it's genetic or coincidental.

Epidermolysis bullosa simplex causes easily blistered skin due to faulty skin cell proteins, leading to new treatment ideas.

DNA profiling in forensics has improved, but predicting physical traits and ancestry from DNA has limitations and requires ethical consideration.

The document concludes that while white skin, nail, and mucosa diseases increase skin cancer risk, they are generally harmless, especially compared to darker pigmentation conditions.

Women treated with X-ray for scalp fungus as children had a higher chance of hair loss, especially with higher radiation doses and severe fungus infections.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

A young man was diagnosed with trichoepitheliomas, causing thick skin and hair loss.

Combination therapies for androgenetic alopecia work best but can have significant side effects and costs.

Strong skin creams work well for long-term scalp inflammation in Rapp-Hodgkin Ectodermal Dysplasia.

Using old drugs for new uses can help treat rare immune deficiencies.

A 16-year-old boy's arm hair grew more after wearing a splint, but it returned to normal in 8 months.

People with Myotonic Dystrophy type 1 are more likely to have certain skin conditions, but not more likely to get skin cancer.

A boy with Pachyonychia congenita has a confirmed gene mutation, highlighting the need for a local genetic database in India.

A man had a benign pilar cyst on his face, which is rare and was successfully removed by surgery.

Eruptive vellus hair cysts are often missed in diagnoses.

New treatments targeting specific genes show promise for treating keratin disorders.

Premature balding in some men may be linked to altered hormones, but it's not the male equivalent to polycystic ovary syndrome or metabolic syndrome.

Patients often experience long-lasting changes to their hair after stem cell transplants.

The document concludes that there are various causes and treatments for hair loss, with hair transplantation being a notable option.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

A woman developed rare, unexplained curly hair on her scalp and eyelashes.

Hair restoration surgery can effectively increase pubic hair density, with patient satisfaction and natural results largely depending on the chosen hair pattern and graft design.

Hair loss in Clouston's syndrome improved with minoxidil and tretinoin treatment.

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.