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Hyperadrenocorticism in ferrets is linked to neutering and indoor housing, and is best treated with surgery and a deslorelin implant.

Androgen therapy can help with symptoms like low libido in women, but more research is needed to understand its long-term safety and effects on health.

Men, particularly those with hair loss, are more likely to get the virus, and those with prostate cancer may have milder symptoms. Testosterone's role in the disease is unclear, and the virus doesn't seem to harm male fertility. Women with PCOS might be at higher risk. More research is needed.

Acne in reproductive-age women may be linked to conditions like PCOS and lifestyle factors, so doctors should check for these when treating acne.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

Skin doctors should know about skin and kidney disease links to prevent serious kidney problems.

Cronkhite-Canada syndrome can be diagnosed without gastrointestinal polyps if there is severe mucosal atrophy and edema.

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

Skin and hair changes in horses can indicate serious diseases, and recognizing these signs is important for treatment and management.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

The document recommends a team-based approach and personalized care for managing diabetes in teenagers.

Using minoxidil and tretinoin on the skin, along with oral vitamin D, improved hair thickness and density in two girls with woolly hair.

Obesity is a major risk factor for insulin resistance in Taiwanese women with PCOS, which is also an independent risk factor for metabolic syndrome.

The review suggests limited treatments for common hair loss conditions, with potential for future improvements.

A rare skin disorder affecting the face was found in a 28-year-old Saudi man.

The conclusion is that different blood diseases cause specific oral symptoms and require varied treatments to manage these symptoms and improve patient health.

Identifying nonclassic congenital adrenal hyperplasia and carriers of CYP21 mutations is challenging, and genetic counseling is recommended due to their prevalence.

The Hair India 2010 conference introduced a new hair loss classification and highlighted advanced diagnostic techniques in trichology.

Activating TLR5 in the gut can extend lifespan and improve health in aged mice.

The symposium highlighted the importance of understanding disease mechanisms for targeted dermatology treatments.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

A cross-bred lamb with severe skin and movement issues had ichthyosis fetalis but normal vitamin A levels.

Removing both ovaries treated the woman's excess male hormone symptoms.

Vitamin B12 deficiency can cause reversible hair color loss in children.

The meeting presented new findings on hair stem cells, pigmentation, genetics, and modern hair treatment techniques.

Premature graying of hair is common and stressful, but not well understood or treated.

Wnt and Shh signaling are key in noggin-induced tumors, and blocking them can slow tumor growth.

A 50-year-old woman with breast cancer developed an autoimmune skin disorder, highlighting the need for thorough checks and team-based treatment.

Pica disorder in central Iraq is mainly found in females and is linked to low iron levels; treatment with iron improves most patients.

Skin infections and rashes are the most common skin problems in children.