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Early and aggressive treatment is crucial for preserving vision in infants with AEC syndrome.

Rapp-Hodgkin syndrome, AEC, and EEC are different expressions of the same genetic disorder caused by TP63 gene mutations.

The infant likely has Hay-Wells syndrome and needs genetic testing and heart screening.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

Strong skin creams work well for long-term scalp inflammation in Rapp-Hodgkin Ectodermal Dysplasia.

Hair, teeth, and mammary glands develop similarly at first but use different genes later.

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

Dermatoscopy is a useful tool for diagnosing hair disorders and can help choose samples for more detailed analysis.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

The document concludes that surgery is a preferred treatment for cicatricial alopecia, with the method chosen based on individual factors and may require multiple sessions and careful postoperative care.

Hair problems can be caused by genetics or the environment, and treatment should focus on the cause and reducing hair damage.

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.

Skin and hair can help us understand organ regeneration, especially how certain stem cells might be used to form new organs.

New treatments and early diagnosis methods for permanent hair loss due to scar tissue are important for managing its psychological effects.

The document emphasizes the importance of correctly identifying and classifying genetic hair disorders to help diagnose related health conditions.

Deleting the p63 gene in certain cells causes problems in thymus development and severe hair loss in mice.

Hair transplants can be a treatment for scarring hair loss if there's good blood flow and no active disease.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

Understanding skin structure and development helps diagnose and treat skin disorders.

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

The meeting highlighted major advances in skin research, including new findings on skin microbes, genetic links to skin diseases, and improved treatments for various conditions.

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.

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

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

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

The document is a detailed guide on skin conditions and treatments for dermatologists.

Proper care and diet are crucial to prevent health issues in gerbils.

Atopic dermatitis may have genetic causes and can be treated with pharmacologic methods, glycerin creams, and controlling Staphylococcus aureus colonization.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

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