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Monilethrix Syndrome causes fragile, beaded hair that breaks easily and needs early diagnosis for better care.

Some hair loss disorders are caused by genetic mutations affecting hair growth.

The document concludes that early diagnosis and treatment are crucial for children with hair loss to prevent permanent damage, although not all conditions can be effectively treated.

Hair shaft dysplasias are abnormal hair conditions that can be inherited or acquired and may signal other health issues, with limited treatment options available.

The review highlights the importance of stem cells in hair health and suggests new treatment strategies for hair loss conditions.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

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

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

Advanced imaging techniques are crucial for accurately diagnosing Monilethrix, a rare hair disorder.

The document explains the diagnosis and characteristics of woolly hair nevus and alopecia neoplastica.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

5% topical minoxidil improves hair density and quality in monilethrix patients.

Monilethrix is a genetic disorder causing brittle hair, diagnosed using tricoscopy.

The document concludes that accurate diagnosis of hair loss in children is crucial due to limited treatment options and the condition's psychological impact.

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

Finasteride, often used for hair loss, can potentially cause cataracts.

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.

Trichoscopy can diagnose monilethrix, a genetic hair defect causing hair thinning and loss.

Puberty often causes skin issues like acne and excessive sweating, and treatments require patience as results may vary.

Telocytes in the scalp may help with skin regeneration and maintenance.

Telocytes might help with skin repair and regeneration.

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.

The patient was diagnosed with oral lichen sclerosus and needs long-term monitoring.

Eye exams are crucial for kids with 13q deletion syndrome, tamoxifen can cause vision loss, Propecia may lead to cataracts, Lipoid Proteinosis causes skin bumps, and OCT is useful for diagnosing macular diseases.

A baby boy with 13q deletion syndrome had eye cancer, a woman's vision improved after stopping a breast cancer drug, a man developed cataracts from using Propecia, and a rare skin disorder called Lipoid Proteinosis was discussed. Also, a tool called OCT is useful for diagnosing macular diseases.

Taking Propecia might lead to the development of cataracts.

The document discusses various eye conditions and their treatments, including a rare eye cancer in a baby, vision loss from a cancer drug, cataracts from a baldness treatment, a rare skin disorder, and a specific type of eye disease diagnosed with a special imaging technique.

Multiple eye conditions were studied, highlighting the importance of various imaging methods for diagnosis, the vision side effects of drugs tamoxifen and Propecia, and the usefulness of optical coherence tomography for diagnosing and monitoring macular and retinal diseases.