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Dermatologists give better information on pathology forms, hypersensitivity vasculitis is a common skin issue, misdiagnoses can occur, and various skin conditions are linked to loss of elastin or genetic factors.

Non-classical 21 hydroxylase deficiency is an underdiagnosed cause of female hair loss and polycystic ovarian syndrome.

The protein called small nuclear ribonucleoprotein polypeptide E is identified as a cause of a type of hair loss without other symptoms.

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

The man was diagnosed with Cronkhite-Canada syndrome, a rare disorder with GI polyps, skin issues, hair loss, and nail problems.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

Mother and son diagnosed with a rare genetic hair loss condition with no effective treatment.

Oral minoxidil and growth factors improved hair density and thickness in a girl with hereditary hair loss.

Surgery may help infants with sagittal craniosynostosis develop more typical language processing.

Higher hs-CRP levels in Indian adolescent women with PCOS are more related to BMI than PCOS itself.

Higher vitamin D levels are linked to higher iron levels in Korean women without metabolic syndrome, but not in those with it.

PCOS is linked to diabetes and insulin resistance, and managing AGEs may help treat related symptoms.

There is no standard treatment for the rare Cronkhite–Canada syndrome, which can be fatal and lead to cancer.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

Early detection and treatment of primary biliary cirrhosis and related autoimmune diseases improve outcomes.

Hirsutism is often caused by high male hormone levels and can be treated with lifestyle changes and medications.

The document explains the genetic causes and characteristics of inherited hair disorders.

Shift nurses show altered body temperature and stress hormone levels, suggesting their body clocks adjust to irregular schedules.

The April 2014 issue of "Fertility and Sterility" discussed various reproductive health topics, including hormone therapy benefits, sperm and genetic factors in male infertility, and the link between PCOS and diabetes.

Low-dose finasteride effectively reduces hirsutism without serious side-effects.

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

Tafluprost could be a potential treatment for hair loss by promoting hair growth phase changes.

The supplement highlighted advancements and challenges in plastic and reconstructive surgery, including the impact of smoking, chemotherapy, and new treatments like Tafluprost for hair loss.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

Metreleptin treatment significantly improved metabolic health in a boy with congenital generalized lipodystrophy.

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

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

Protoporphyrin IX is useful in cancer treatment but can cause health problems if not properly regulated.