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Get head MRI for babies with achondroplasia early, use free immunoglobulin light chains to detect certain neurodevelopmental disorders, and video calls work for speech therapy in patients with facial anomalies.

Dentists should start preventive treatments early for children with Ichthyosis Vulgaris to avoid dental problems.

The document concludes that permanent hair loss conditions are complex, require early specific treatments, and "secondary permanent alopecias" might be a more accurate term than "secondary cicatricial alopecia."

A mushroom extract might reduce hair loss and liver damage caused by certain chemotherapy drugs in animals.

Congenital Adrenal Hyperplasia is a rare inherited disease causing hormone imbalances, affecting growth, fertility, and heart health, diagnosed through blood tests and treated with medication and lifestyle changes.

EDA signaling is linked to skin disorders, various cancers, and liver disease.

The AVET system effectively delivers genes to human keratinocytes and may help treat skin diseases.

Treating non-classic congenital adrenal hyperplasia is complex because the benefits of hormone treatment must be weighed against potential health risks.

A girl with type 1 diabetes developed a serious eye condition very early, suggesting the need for earlier eye checks and that early treatment can work well.

The document concluded that more research is needed to understand how estrogen affects the enzyme involved in hirsutism development.

A 31-year-old woman was diagnosed with Complete Androgen Insensitivity Syndrome much later than usual, leading to a call for earlier detection and treatment guidelines.

A woman was diagnosed with porphyria cutanea tarda and improved with phlebotomy and lifestyle changes.

Mutations in the AR gene cause hair thinning and loss.

Birt–Hogg–Dubé syndrome is a rare genetic condition causing skin lesions, lung cysts, and a higher chance of kidney cancer.

Epidermolysis bullosa simplex causes easily blistered skin due to faulty skin cell proteins, leading to new treatment ideas.

Pediatric endocrinologists should provide early fertility counseling and preservation options to young patients at risk of infertility.

Recent progress has been made in understanding inherited hair and nail disorders.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.

The conclusion is that proper evaluation and treatment of hair loss in midlife women is important, considering the emotional impact and potential for various treatments.

Two treatments for male pattern hair loss are minoxidil and finasteride, but they have side effects and may not satisfy everyone.

Early diagnosis and a combination of treatments, including minoxidil and finasteride, are recommended for managing hair loss in India.

Polycystic Ovary Syndrome (PCOS) is a common but often undiagnosed disorder in women that can cause irregular periods, infertility, and other symptoms, and can be managed with lifestyle changes, medication, and sometimes surgery.

Infertile men are more likely to produce sperm with abnormal chromosome numbers, which can affect pregnancy success and embryo health.

M30 is a promising treatment for preventing hair loss during chemotherapy.

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

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

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

Treat genetic hair loss early with FDA-approved medications and consider hair transplantation.

Many dermatologists believe finasteride can cause sexual side effects and counsel patients about them.

Careful planning and patient counseling can lead to excellent hair transplant results, often in one or two sessions.