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The document reports unique growth lines in a child after Stevens-Johnson syndrome, skin reaction from parsnips and sun in a girl, and itchy skin with xanthomas in a boy with Alagille syndrome.

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 document concludes that proper diagnosis and treatment of hair shaft disorders require understanding their unique causes and avoiding hair-damaging practices.

The document concludes that proper diagnosis and management of hair loss in children require a detailed examination and understanding of various hair disorders.

The document concludes that proper recognition and treatment of skin appendage disorders are important for management.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

Hair changes can indicate systemic diseases or medication effects.

The study found that specific proteins are markers of hair follicle development in human fetuses.

Male pattern hair loss is genetic and influenced by hormones, with treatments like minoxidil and surgery available.

The reconstructed skin model from hair follicles functions like human skin in processing chemicals and can be used to test ingredient safety.

Hair microscopy is a simple and cost-effective method to help diagnose systemic diseases in children.

S5αR inhibitors might help treat schizophrenia and other mental disorders but need more research.

Correct diagnosis and treatment are crucial for effective management of lipid storage myopathies.

UVB is good for a skin condition in Asian kids, a lotion works for head lice, a drug helps with a skin blistering disorder, a foam reduces itchiness in skin inflammation, birthmarks can be more widespread, and criteria for a neurocutaneous disorder were agreed upon.

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

Human skin produces sex hormones like estrogen and testosterone, influenced by ARO and StAR, which may affect skin elasticity and hair growth.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

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

Epidermolytic ichthyosis can be inherited in a semidominant way with mild symptoms in carriers.

Natural gene therapy shows promise for treating skin disorders like epidermolysis bullosa.

Oral isotretinoin temporarily improved skin symptoms in a child with IFAP syndrome.

Tigason improved hair growth in a boy with monilethrix without side effects.

The document explains how to identify different hair problems using a microscope.

Hair and nails are similar keratin structures with different shapes and growth, affected by the same diseases and environmental factors.

A child with Olmsted syndrome showed mild improvement in hair and skin issues with treatment.

Retinoids are effective for various skin conditions and hair loss but have serious side effects, so low doses are recommended.

The study found no common cause for a girl's crystalline cataract and uncombable hair, suggesting their co-occurrence might be coincidental.

A specific gene mutation causes Olmsted syndrome.

Steatocystoma multiplex causes recurring skin cysts and needs early recognition for better management.

Keratin is crucial for keeping skin cells healthy and its changes can lead to diseases and affect cell behavior.