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The document concludes that understanding nail anatomy is key for diagnosing nail diseases, early signs of nail melanoma may allow for less aggressive treatment, and specific genetic mutations are important in thyroid cancer prognosis and treatment.

A family got a fungal infection from a boy who had contact with rabbits, but they all recovered with treatment.

Acrodermatitis enteropathica is a rare inherited disorder causing skin issues, diarrhea, and hair loss.

Cronkhite-Canada syndrome can cause multiple gastrointestinal polyps and various physical symptoms.

A man's scalp condition was misidentified as hair loss dots but was actually a common follicular disorder.

No treatment alters the natural progression of alopecia areata, and effectiveness varies, with some possibly working better in children.

The article concludes that while we understand a lot about how melanocytes age and how this can prevent cancer, there are still unanswered questions about certain pathways and genes involved.

Severe hair loss links to metabolic issues in older men with psoriasis.

Women with excessive hair growth often have hormonal issues and need medical advice and treatment.

Male pattern hair loss is diagnosed and treated earlier and is milder, possibly due to early puberty.

PCOS is linked to metabolic issues and infertility, needing more research.

Hidradenitis suppurativa may be a type of autoinflammatory skin disease linked to gene mutations and immune system issues.

Children with different rheumatologic diseases have specific skin symptoms that can help with diagnosis.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

Faulty Notch signalling may cause hair follicle changes and inflammation in hidradenitis suppurativa.

Two boys had a rare skin condition needing to be differentiated from similar disorders, with unclear inheritance due to few cases.

FFA's causes may include environmental triggers and genetic factors.

Balding in men is strongly linked to high blood pressure and family history.

Finasteride can cause serious emotional side effects; doctors should check patients' mental health history before prescribing.

Brothers of women with PCOS tend to have higher levels of a hormone called DHEAS, indicating a possible genetic link.

Loose anagen hair can appear at any age and may improve over time.

Alopecia areata, a type of hair loss, is likely an autoimmune disease with a genetic link, but its exact cause is still unknown.

The report described a unique case of Cronkhite-Canada syndrome with unusual polyps and an association with multiple myeloma.

Pseudopelade is a rare inherited hair loss condition with a genetic cause.

DPCP treatment for alopecia areata can sometimes cause vitiligo.

The cause of alopecia areata is likely a mix of genetics, immune system issues, and environmental factors, with more research needed to understand it fully.

Some patients with high prolactin levels don't show symptoms because they have a form of the hormone that's less active.

An 8-year-old boy with hair-pulling disorder had a bald patch that was confirmed not to be a fungal infection and was treated with therapy.

A man with Cronkhite-Canada syndrome had all 20 nails detach but improved with treatment.

The document says that hair loss in women is often due to androgenic alopecia, similar to male baldness, and that hirsutism is treated with hormonal and cosmetic methods.