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The document concludes that hair loss in cats is caused by various factors, including allergies, mites, infections, and hormonal issues, with treatments varying accordingly.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

Marie-Unna Hereditary Hypotrichosis is a rare genetic condition causing sparse hair growth, requiring specific recognition for proper care.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

A gene mutation causes woolly hair in a Syrian patient.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

CaBP1 and CaBP2 are important for continuous hearing by preventing inactivation of calcium currents in ear cells, with CaBP2 also able to restore hearing when reintroduced.

The conclusion is that differentiating wound types in RDEB patients is important for clinical trials and understanding the disease.

Foam corticosteroid covers as well as traditional forms.

The document concludes that ongoing research using animal models is crucial for better understanding and treating Alopecia Areata.

A specific gene mutation causes varying hair loss severity in a Pakistani family.

Monilethrix is a rare genetic hair disorder that's hard to treat.

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

The document concludes that alopecia areata is an autoimmune disease without a definitive cure, but treatments like corticosteroids are commonly used.

The document says that treating the root cause of hair follicle damage is crucial to prevent permanent hair loss, and treatment options vary.

Fat tissue stem cells may help increase hair growth.

Bariatric surgery affects skin health, causing both direct complications and changes in existing skin conditions, often related to nutritional deficiencies.

Early and personalized treatment for hair loss in young people is crucial to prevent permanent damage and should include psychological support.

Treating non-classic congenital adrenal hyperplasia is complex because the benefits of hormone treatment must be weighed against potential health risks.

A rabbit with sebaceous adenitis was effectively treated with ciclosporin and medium-chain triglycerides.

Papillon-Lefèvre Syndrome causes early tooth loss and skin issues, needing early dental diagnosis.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

The conclusion suggests a new way to classify bradykinin-mediated angio-oedema based on different causes and its possible link with urticaria, which could improve diagnosis and treatment.

Cats lose fur due to various reasons, including allergies, infections, genetics, hormones, diet, cancer, stress, and some conditions are treatable while others are not.

Skin problems are common after stem cell transplants, and early treatment by dermatologists can improve patient outcomes.

An infant with seizures and hair loss was diagnosed with biotinidase deficiency and treated successfully with biotin.

Doctors should consider Netherton syndrome in patients with chronic skin and hair issues to avoid misdiagnosis.

Stress, nutritional issues, and chronic diseases can cause hair loss, and nail changes may signal internal diseases; treatment focuses on the underlying cause.

A five-month-old boy with Omenn syndrome successfully recovered after a stem cell transplant with reduced intensity conditioning.

The document concludes that permanent hair loss conditions are complex, require early specific treatments, and "secondary permanent alopecias" might be a more accurate term than "secondary cicatricial alopecia."