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Trichoscopy is a useful tool for diagnosing hair disorders without pulling out hair.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

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

Hair loss in black women needs more research, early intervention, and community education.

The study found no common cause for a girl's crystalline cataract and uncombable hair, suggesting their co-occurrence might be coincidental.

Premature balding in some men may be linked to altered hormones, but it's not the male equivalent to polycystic ovary syndrome or metabolic syndrome.

Minoxidil 2% effectively treats Monilethrix without side effects.

Looking at skin can help find and treat serious diseases early.

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

Reflectance confocal microscopy is a useful, non-invasive tool for diagnosing some skin diseases, with potential for future improvements.

Hair loss in Clouston's syndrome improved with minoxidil and tretinoin treatment.

Male pattern baldness involves hormone-related hair thinning, shorter hair, and inflammation.

New treatments targeting the Hedgehog pathway can help treat advanced skin cancer but may have side effects and their effectiveness in early stages is unknown.

Some congenital hair disorders improve with age and can be managed with treatments like minoxidil, retinoids, supplements, and gentle hair care, but there's no cure.

Researchers found a gene mutation responsible for a rare hair loss condition.

A new mutation in the HR gene causes hair loss in a specific family.

Minoxidil 5% solution significantly improved hair density in a girl with loose anagen hair syndrome over 28 months, with no side effects.

Minoxidil effectively promotes hair regrowth in younger patients with small balding areas.

Hair restoration surgery can effectively increase pubic hair density, with patient satisfaction and natural results largely depending on the chosen hair pattern and graft design.

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.

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

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.

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

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

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 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.