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People with hypohidrotic ectodermal dysplasia are more likely to experience long-term fatigue and hair loss after COVID-19.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

Skin changes are key for early diagnosis and treatment of rheumatic diseases.

Mycophenolate mofetil helped reduce steroid use in treating a dog's autoimmune skin disease.

Toxic Epidermal Necrolysis is a rare, serious skin condition that can affect anyone, is more common in women, and may be linked to genetics, with a 20% mortality rate mainly due to sepsis.

The meeting discussed medical findings, including benefits of certain treatments for cancer and heart conditions, and highlighted issues like poor adherence to preventive measures and skill gaps among interns.

APS-1 in Italy shows diverse AIRE mutations and various autoimmune issues.

Eyelashes protect the eyes, but more research is needed to understand how.

The document concludes that parathyroid diseases have a range of clinical features and outcomes, with some conditions being treatable and others having a high risk of mortality.

Myrtle has various health benefits and potential for medicine development.

In 2002, various skin reactions were reported due to different drugs, including allergies, hair loss, skin lesions, and other skin conditions.

Genetic screening is crucial for accurately diagnosing APS-1 due to its varied symptoms.

People with atopic dermatitis are more likely to develop other skin conditions due to shared genetics and immune pathways.

Ketoconazole cream is effective for skin conditions like seborrheic dermatitis and may help with hair loss and other skin issues, with generally mild side effects.

Cosmetics and procedures can cause eye issues, from mild discomfort to serious conditions, due to allergies, toxins, or poor care.

The document concludes that eyelash trichomegaly, which is the abnormal growth of eyelashes, can be present from birth, caused by diseases, or result from certain medications.

Using bimatoprost on one side of the face caused increased cheek hair growth in a patient.

St. John's Wort extract and oil safety in cosmetics is unclear; more data needed on photosensitization, toxicity, and human irritation.

Non-immune factors play a significant role in alopecia areata.

Using bimatoprost on one side of the face caused increased cheek hair growth in a patient.

The document concludes that changes in eyelashes and eyelid skin can indicate various local and systemic diseases.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

The document concludes that periocular hair disorders have various causes and treatments, and proper evaluation by specialists is important for management and prognosis.

A man with KID syndrome developed a rare cancer in a long-term skin infection.

An 11-year-old girl with a rare skin disorder also had cornea issues and dry eye, needing careful management.

AA patients with comorbid conditions face more severe hair loss and need specific treatments.

People with alopecia areata have similar retinal structures but thicker choroidal regions compared to those without the condition.

Long eyelashes in a patient were an unusual sign of systemic lupus erythematosus.

The document describes a rare case of IFAP syndrome, a genetic condition with symptoms of hair loss, light sensitivity, and scaly skin.

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