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CCCA is a common hair loss condition in African American women, often inherited and influenced by hairstyling, with unique scalp features detectable by special tools.

A boy with chromosome 13q deletion syndrome developed eye cancer, a woman with breast cancer lost vision due to a rare side-effect of her treatment, a man's vision worsened after using a hair loss drug, and two rare disorders were discussed. Optical Coherence Tomography is useful for diagnosing and monitoring these conditions.

The document concludes that Syndromes of Severe Insulin Resistance are rare disorders with limited treatment options.

People with Mucopolysaccharidoses often have skin problems like thick skin and extra hair, and recognizing these can help diagnose and treat the condition early.

Temporal triangular alopecia is a lifelong condition with hairless patches on the side of the head that may be present from birth.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

The document concludes that scalp disorders can be treated with hair washing, specific shampoos, medications, and sometimes surgery or hair transplants, but hereditary baldness is untreatable.

Different human traits like skin color and hair type vary between populations due to genetic adaptations to the environment.

The document concludes that the girl's hairlessness is likely inherited from her parents.

Children's hair loss can be caused by many factors, including autoimmune diseases, emotional stress, genetics, and infections, with treatment and prognosis varying.

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

Hirsutism can be caused by various conditions besides PCOS, and it's important to treat the underlying issue and manage symptoms with medication and cosmetic approaches.

Sebaceous glands are involved in various skin disorders, some treatable with medications like finasteride and minoxidil.

Steroid Sulfatase inhibitors show promise in treating hormone-dependent disorders like cancers, hair loss, and acne, with 667COUMATE being a potential candidate for breast cancer treatment trials.

The document concludes that inherited epidermolysis bullosa is a challenging genetic condition requiring multidisciplinary care and new treatments.

Iron supplements may reverse premature graying in iron-deficient individuals; ingrown nails are common in diabetics with certain risk factors; topical finasteride may reduce scalp DHT as effectively as oral finasteride; monilethrix treatment is challenging but some medications can help.

Changes in testosterone and estrogen receptor genes can affect how men age, influencing body fat, hair patterns, and possibly leading to skin disorders.

The chapter explains that there are many genetic skin disorders affecting skin cell formation, including both common and rare types.

Older adults often have skin problems due to aging, and treating these conditions requires attention to both physical and mental health.

Melanocytes produce melanin; their defects cause vitiligo and hair graying, with treatments available for vitiligo.

Male hormones and their receptors play a key role in hair loss and skin health, with potential new treatments being explored.

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

AFM helps study hair surfaces for dermatology, cosmetics, and forensics.

The document concludes that early recognition and treatment of PCOS in adolescents is crucial for managing symptoms and long-term health risks.

Skin abnormalities can indicate immunodeficiency due to shared origins with the immune system.

Two rare genetic diseases cause severe rickets in children due to defects in vitamin D metabolism.

Hirsutism is too much hair growth in women like the pattern in men, often caused by high male hormones, and can be treated with hormone control and hair removal methods.

The girl's unexpected pubic hair growth led to a diagnosis different from complete androgen insensitivity syndrome.

Nearly half of children with primary immunodeficiency disorders showed skin problems, often as the first sign of their condition.

Targeting androgen receptors could be a promising way to treat skin disorders with fewer side effects.