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Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.

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

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

Scientists successfully created mouse hair proteins in the lab, which are stable and similar to natural hair.

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

A male with aromatase deficiency improved bone health with estradiol treatment.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

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

Long-term use of difluprednate eye drops in dogs can lead to hair loss and hormone imbalance.

Foxp3 is crucial for regulatory T cell function, and targeting these cells may help treat immune disorders.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

The meeting highlighted the genetic basis of female pattern hair loss and various skin health insights.

The study suggests that a specific gene variation and higher gene activity are linked to increased baldness in Egyptian men.

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

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

Infertile men are more likely to produce sperm with abnormal chromosome numbers, which can affect pregnancy success and embryo health.

People with myotonic dystrophy type 1 have a higher chance of getting skin tumors, including melanoma.

DNA phenotyping helps predict physical traits from DNA with varying accuracy and requires careful ethical and legal handling.

A new non-invasive method can analyze skin mRNA to understand skin diseases better.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

Hair follicles in the back of the rosette fancy mouse have reversed orientations due to a gene mutation.

Most adrenal cortex tumors are benign and non-secreting, but proper diagnosis and treatment are important due to the rare possibility of cancer.

Permanent hair dyes use chemicals that react with hydrogen peroxide to create color.

Different human traits like skin color and hair type vary between populations due to genetic adaptations to the environment.

There is no cure for myotonic dystrophy type 1, so treatment focuses on managing symptoms and complications.

Acne is linked to inflammation and insulin resistance, and is associated with various syndromes that require different treatments.

Pattern baldness is likely caused by a dominant gene influenced by testosterone levels, making it more common in men.

The conclusion is that many small genetic variations influence claw disorders in cows, and using genomic selection could help reduce these disorders.

New method finds genetic links between Type 2 Diabetes and Prostate Cancer not seen before.

Genes and epigenetic changes are important in the development of Polycystic Ovary Syndrome.