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New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

The document emphasizes the importance of correctly identifying and classifying genetic hair disorders to help diagnose related health conditions.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

Many potential alopecia treatments need more testing to confirm they promote acceptable hair growth with minimal side effects.

Lack of cystatin M/E causes thin hair and dry skin.

A mutation in the FAM83G gene is linked to skin and hair abnormalities in two related individuals.

People with myotonic dystrophy type 1 tend to develop basal cell carcinoma at a younger age but not more frequently than others.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

PRP helps hair growth in common hair loss disorder.

Low-dose oral minoxidil increases hair thickness and length in children with a hair disorder called Loose Anagen Hair Syndrome.

Children with classic congenital adrenal hyperplasia have thicker heart fat and are at higher risk for heart problems and early atherosclerosis.

Skin abnormalities can indicate immunodeficiency due to shared origins with the immune system.

Scientists have found specific genes linked to different hair loss conditions, which could lead to new treatments.

A woman with a rare type of dermatomyositis improved with low-dose prednisone and methotrexate.

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

Vismodegib is effective for basal cell carcinoma but has severe side effects.

People with Mucopolysaccharidoses often have skin problems like thick skin and extra hair, and recognizing these can help diagnose and treat the condition early.

People with Myotonic Dystrophy type 1 are more likely to have certain skin conditions, but not more likely to get skin cancer.

A new mutation in the AGPAT2 gene causes severe fat tissue loss and related health issues by reducing the protein's levels.

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

A specific thyroid hormone resistance mutation may be linked to different types of hair loss.

Women with myotonic dystrophy might get diseases related to male hormones because their body tissues are extra sensitive to these hormones.

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

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.

Smoking increases early hair loss risk in men; quitting may help prevent it.

BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

Simvastatin may help manage symptoms in women with non-classic congenital adrenal hyperplasia by lowering cholesterol and certain hormone levels.

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

A rare skin disorder, Ichthyosis with confetti, has no cure but treatment focuses on managing symptoms with moisturizers.

A woman's hair turned gray and fell out after starting a cancer drug called imatinib mesylate.