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Toxic Shock Syndrome mainly affects menstruating women, can recur, and is linked to staph bacteria, with rapid treatment being crucial.

The study found that Keratosis Pilaris Atrophicans is a genetic skin condition that starts in childhood, involves inflammation and scarring, and current treatments are only somewhat effective.

Toxic Shock Syndrome progresses quickly, often involves multiple organs, and is linked to Staphylococcus aureus toxins, with treatment options available but diagnostic challenges remaining.

The document concludes that accurate diagnosis is crucial for effectively treating common scalp disorders, which often have similar symptoms.

People with HIV and low T cell counts have more hair and scalp problems.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

Medication and hair removal methods can improve hirsutism, but no drugs were specifically approved for it in North America as of 1995.

Taking tamsulosin or finasteride and being older increase the risk of floppy iris during cataract surgery.

Most treatments for hair loss in 1997 were not effective for most people, and maintaining hair growth was difficult.

Some cases of folliculotropic mycosis fungoides may progress slowly and not need aggressive treatment.

The study found that treatment improved hair condition in patients with Fibrosing Alopecia in a Pattern Distribution in Chile.

Taking Propecia might lead to the development of cataracts.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

The study concludes that early diagnosis of Frontal Fibrosing Alopecia is important, as it is often found in postmenopausal women, may be related to Lichen Planopilaris, and eyebrow hair loss is a common sign.

Norwegian puffin dogs have a unique type of hair loss that often doesn't get better on its own and responds well to ciclosporin treatment.

Temporal triangular alopecia in infants is mostly seen in males at birth, with unique features that help with diagnosis.

Breast cancer hormone therapy can cause hair loss, which can be treated with daily applications of specific topical solutions like minoxidil and hydrocortisone butyrate.

Narrowband-UVB phototherapy successfully treated a rare case of Graham Little-Piccardi-Lassueur syndrome.

Hypothyroidism patients with hair loss typically have thinning hair, smaller hair follicles, and normal hair shedding.

Early diagnosis and proper treatment improve outcomes for methylmalonic acidemia.

Most children with a common hemochromatosis genotype had elevated iron levels but no severe symptoms.

Some overweight or obese men with long-term frontal fibrosing alopecia may have abnormal sex hormone levels.

Japanese cases of fibrosing alopecia show a unique age and hair loss pattern, possibly due to racial differences.

Neutered ferrets often develop hyperadrenocorticism, with symptoms like hair loss and lethargy, and androstenedione is a key indicator for diagnosis.

Most women aged 20-40 in the study lost hair diffusely and in volume over 6 weeks to 6 months, mainly due to telogen effluvium, often without a clear cause.

This type of hair loss is probably often missed and treatments reducing inflammation might work well.

The guidelines suggest using various treatments, including antidepressants and steroids, for alopecia areata and discuss the condition's genetic and immune aspects.

Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.

Frontal Fibrosing Alopecia mainly affects postmenopausal Mexican women, requiring early detection to prevent permanent hair loss.

Most patients with autoimmune blistering diseases experienced some hair loss, which may be underreported and linked to disease severity.