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Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

The document is a detailed medical reference on skin and genetic disorders.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

CD61 is important for mouse tooth cell growth and works through Lgr5.

Early development of hair, teeth, and glands involves specific signaling pathways and cellular interactions.

Patients with Shwachman-Diamond syndrome often get misdiagnosed due to a wide range of symptoms, including immune system problems and bone abnormalities.

Diabetes can lead to blindness and skin problems, and managing blood sugar and blood pressure is crucial to prevent these complications.

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

The document reviews various hair and nail disorders, their causes, and treatments, emphasizing the need for proper diagnosis and the link between nail changes and systemic diseases.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

The document explains various skin conditions and their treatments.

Dermatopathia pigmentosa reticularis causes skin discoloration, hair loss, and nail problems.

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

Odontogenic keratocysts are caused by abnormal Hedgehog signaling and can lead to tooth and bone issues.

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

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

The document concludes that Functional Hypothalamic Amenorrhea should be carefully diagnosed and managed to prevent health complications, using lifestyle changes and specific medications.

Acne in children varies by age and severity, requires a pediatric treatment approach, and may need diagnostic evaluation for underlying conditions.

Certain micronutrients may improve hair and nail health, but more research is needed to confirm their benefits.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

Dates may improve heart health, fight infections, protect kidneys, reduce inflammation, support pregnancy, promote dental and bone health, enhance mental function, and have anti-cancer properties, and are also beneficial for skin and hair care.

Survivors of Stevens-Johnson syndrome/toxic epidermal necrolysis need ongoing care for various long-term health problems.

Good nutrition is crucial for health and preventing disease, and supplements can help prevent nutrient deficiencies.

Mice lacking fibromodulin have disrupted healing patterns, leading to abnormal skin repair and scarring.

TNF family proteins are crucial for the development of skin features like hair, teeth, and mammary glands.

The TGF-β family helps control how cells change and move, affecting skin, hair, and organ development.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.