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

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

Monilethrix causes different levels of hair loss in family members.

The symposium highlighted the importance of understanding disease mechanisms for targeted dermatology treatments.

The study found that Keratosis Pilaris Atrophicans is a genetic skin condition that starts in childhood, involves inflammation and scarring, and current treatments are only somewhat effective.

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

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

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."

The document concludes that understanding hair biology and recognizing hair conditions are crucial for managing and treating hair loss in children.

The document concludes that proper diagnosis and management of hair loss in children require a detailed examination and understanding of various hair disorders.

The document concludes that proper recognition and treatment of skin appendage disorders are important for management.

Cancer survivors often experience worse skin problems from treatment than expected, and working with dermatologists could help improve their condition.

European guidelines recommend regular eye and ear exams, skin care, vitamin D supplements, and cautious use of medications for managing congenital ichthyoses.

Keratin protein production in cells is controlled by a complex system that changes with cell type, health, and conditions like injury or cancer.

Some children are born with unusually short, fine hair because their hair growth phase is short, but this often gets better by itself during puberty.

Children's hair loss can be caused by many factors, including autoimmune diseases, emotional stress, genetics, and infections, with treatment and prognosis varying.

Hair loss has many causes and treatments, and losing some hair daily is normal; proper diagnosis is key, and minoxidil can help treat it.

Benign skin tumors need accurate diagnosis to ensure proper treatment.

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

Hair loss improved with treatment and successful transplant.

The baby’s hair loss was due to a rare genetic condition, not treatable by usual methods.

Skin changes during pregnancy are common, and non-invasive imaging is safe for monitoring these changes.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

Microneedles improve drug delivery in various body parts, are safe and painless, and show promise in cosmetology, vaccination, insulin delivery, and other medical applications.

Ellis van Creveld syndrome, a rare genetic disorder, can cause unexpected abnormalities in various body organs, requiring thorough patient evaluations.

The document concludes that while there are various treatments for Alopecia Areata, there is no cure, and individualized treatment plans are essential due to varying effectiveness.

A 2-year-old boy had no hair and unusual organ placement, and it's unclear if it's genetic or coincidental.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

Topical PUVA and tacrolimus ointment can effectively and safely treat infant alopecia universalis.

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