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Adults with Tatton-Brown-Rahman syndrome may have serious heart problems and need lifelong heart monitoring.

Lichen Planus is a less common condition affecting skin and mucous membranes, with various types and associated risk factors, challenging to diagnose, significantly impacts life quality, and may have a risk of cancerous changes in oral lesions.

Male pattern baldness is often genetic and linked to a hormone, with treatments like finasteride and minoxidil being effective for some men.

Low-cost dermoscopes can effectively diagnose early female pattern hair loss.

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

An 80-year-old man's deep beard infection was cured with oral terbinafine after identifying the fungus Trichophyton verrucosum.

HLA-DRB5 and other genes may be linked to alopecia universalis.

Using hemocoagulase with platelet-rich plasma in hip replacement can lessen blood loss and improve healing and blood clotting.

A child with trichothiodystrophy also had autoimmune thyroiditis and anemia, which is a new finding.

Mild essential fatty acid deficiency can cause health issues and is worsened by low-fat diets.

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

Nonclassic congenital adrenal hyperplasia is a genetic disorder causing hormone imbalances, affecting fertility and requiring personalized treatment.

The conclusion is that a thorough approach is needed to diagnose and manage hyperandrogenism in teenage girls, recognizing its major psychological and health effects.

Frontal fibrosing alopecia in families shows similar signs to individual cases and may have a genetic link.

Trichoscopy effectively diagnoses early female hair loss, but may need scalp biopsy for confirmation.

A 23-year-old woman's missed periods were caused by a rare genetic disorder treated with hormone patches.

Hair loss caused by genetics and hormones; more research needed for treatments.

Polycystic Ovary Syndrome likely starts in childhood and may be genetic and influenced by early hormone exposure.

Any medication can cause skin reactions, some due to allergies and others due to dosage or genetic factors.

Pediatric systemic lupus erythematosus is a severe autoimmune disease in children requiring early diagnosis and comprehensive management.

Vitiligo is linked to autoimmune diseases and hearing issues, so hearing tests are recommended for patients.

Skin changes are key for early diagnosis and treatment of rheumatic diseases.

A baby was diagnosed with IFAP syndrome due to a new genetic mutation, showing severe skin and developmental issues.

Longer CAG and GGN repeats increase alopecia risk, but no significant link to post-finasteride syndrome found.

The study concluded that Acral lick dermatitis is most common in young male Labrador retrievers, often caused by psychological factors, and leads to skin inflammation and stress-related blood changes.

A young woman with late-stage Vogt-Koyanagi-Harada disease was successfully treated at a hospital.

Hair loss in androgenetic alopecia is caused by genetic factors and androgen excess, and can be treated with combined therapies.

Polycystic ovarian shape is a genetic sign of PCOS and its hormonal and metabolic features can be inherited.

Thiopurines help treat IBD but require genetic testing to avoid side effects.

DFMO treatment improves hair growth, muscle tone, and development in Bachmann-Bupp syndrome patients.