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CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

Gene variation affects prostate issues and hair loss.

A new type of rapid hair loss called ADTA usually gets better on its own within 6 months.

Female pattern hair loss diagnosed by scalp appearance, treated with combined therapies and targeted approaches.

Notch signaling disruptions can cause various skin diseases.

5α reductase type 2 enzyme mutation and oxidative stress may increase androgenetic alopecia risk in Egyptians.

Skin problems can be caused or worsened by physical forces and pressure on the skin.

The document concludes that careful diagnosis is crucial for chromosome 13q deletion syndrome, tamoxifen can cause reversible eye damage, finasteride may be linked to cataracts, and OCT is useful for diagnosing macular diseases.

A man with hypoparathyroidism had other health issues that led to a diagnosis of a rare autoimmune disorder, APS-1.

People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

A man had a large, rare cyst in his mouth removed after 10 years, which fixed his swallowing and breathing problems.

Lack or blocking of SRD5a, a key component in hormone creation, can lead to conditions like pseudohermaphrodism and affect hair growth, bone mass, muscle strength, and reproductive health. More research is needed on its regulation from fertilization to adulthood.

The document concludes that for hair and feather growth, it's better to target the environment around stem cells than the cells themselves.

Premature ovarian insufficiency (POI) can harm women's sexual health, and they may benefit from hormone therapy and counseling.

People with polycystic ovary syndrome (PCOS) are more likely to have higher levels of depression and anxiety, but their personality traits are similar to those without PCOS.

Acne can appear or persist in adulthood due to hormonal changes, external factors, or substance use, and requires appropriate treatment.

The research found that male pattern hair loss is mostly genetic and involves hair thinning due to hormonal effects and changes in gene expression.

Certain mutations in the PADI3 gene may increase the risk of developing a type of scarring hair loss common in women of African descent.

Using rodents for research shows that health problems in the womb can cause diseases later in life.

Men with vertex baldness may have a higher risk of developing prostate cancer, but more research is needed to confirm this.

Baldness in men with prostate cancer is linked to higher levels of certain sex hormones, but chest hair density is not.

The case shows the difficulty in diagnosing certain conditions when standard tests are negative.

Patients with mycosis fungoides have a higher risk of heart disease.

Genetic factors and diet significantly increase the risk of male pattern baldness.

Understanding hair growth involves complex factors, and more research is needed to improve treatments for hair loss conditions.

More adolescent girls in urban areas of India have Polycystic Ovary Syndrome compared to those in rural areas.

New oral treatment, finasteride, effectively and safely treats common hair loss.

The conclusion is that future hair loss treatments should target the root causes of hair thinning, not just promote hair growth.

Many patients experienced hair loss after COVID-19, with women affected more, starting on average 49 days post-infection.

Hair loss may signal metabolic problems and increased risk of heart disease, suggesting people with hair loss should be checked for these issues.