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Genomic profiling for myeloid cancers can find important inherited mutations, but it's challenging when these mutations aren't related to the patient's symptoms.

Certain mutations in the PADI3 gene may increase the risk of developing a type of scarring hair loss common in women of African descent.

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

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

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

Keratin proteins are crucial for healthy skin, but mutations can cause skin disorders with no effective treatments yet.

The dog had sebaceous adenitis, treated with ciclosporin, leading to some hair regrowth.

Gene linked to common hair loss found, may lead to new treatments.

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

The best animal model for studying male-pattern baldness is the stumptailed macaque, not rats or mice.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

Follicle Stimulating Hormone is important for fertility.

Keratin 26 affects cashmere goat hair growth and is influenced by various treatments.

Liver transplantation is a viable option for children with propionic acidemia, improving quality of life and diet, but does not remove all risks and long-term brain outcomes are uncertain.

Polycystic ovary syndrome and iron overload share similar symptoms and can be potentially treated with blood removal, diet changes, and probiotics.

The 2015 Hair Research Congress concluded that stem cells, maraviroc, and simvastatin could potentially treat Alopecia Areata, topical minoxidil, finasteride, and steroids could treat Frontal Fibrosing Alopecia, and PTGDR2 antagonists could also treat alopecia. They also found that low-level light therapy could help with hair loss, a robotic device could assist in hair extraction, and nutrition could aid hair growth. They suggested that Alopecia Areata is an inflammatory disorder, not a single disease, indicating a need for personalized treatments.

Early diagnosis of alopecia frontal fibrosante is crucial, but treatment remains controversial and varies.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

Frontal Fibrosing Alopecia's cause is unclear, affects mainly postmenopausal women, and current treatments focus on stopping hair loss rather than regrowth.

Mutations in mitochondrial DNA might significantly contribute to the development of Polycystic Ovarian Syndrome.

Metformin taken during pregnancy increases SHBG in newborns but doesn't change other hormone levels in mothers or babies.

AGA increased yearly, type I most common, and family history and seborrheic dermatitis often linked.

Androgenic Alopecia, a common hair loss condition, can be effectively treated with finasteride and other treatments.

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

Familial frontal fibrosing alopecia is rare, mostly affects women, and often occurs between sisters or mother-daughter pairs.

Bioengineering can potentially treat hair loss by regenerating hair follicles and cloning hair, but the process is complex and needs more research.

Hair loss in men is common, treatable, but not curable.

Hair loss is caused by genetics and hormones, diagnosed through examination and biopsy, and treated with medications or surgery.

Two treatments for male pattern hair loss are minoxidil and finasteride, but they have side effects and may not satisfy everyone.