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Clouston syndrome is inherited in an autosomal dominant pattern and caused by a specific gene mutation, with no current treatment available.

Loose Anagen Syndrome causes easy-to-pull, thin hair, mainly in young girls, and improves with age.

A baby girl has a hair disorder called monilethrix, causing fragile hair that may improve over time.

A 19-month-old boy with a rare hair disorder showed mild improvement with treatment, but his family chose gentle hair care due to limited success.

A teenager's hair with alternating white and dark bands, known as Pili annulati, is a genetic condition that is usually harmless and often considered attractive.

A girl inherited excessive body hair from her mother and grandmother.

Monilethrix causes different levels of hair loss in family members.

KFSD is a genetic disorder causing hair loss and skin issues, with no effective treatment.

Monilethrix is a genetic disorder causing brittle hair, diagnosed using tricoscopy.

Dogs with dermatomyositis, especially Collies and Shetland Sheepdogs, need better treatments for their skin and muscle inflammation.

The document explains the genetic causes and characteristics of inherited hair disorders.

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

An 11-year-old girl with a rare skin disorder also had cornea issues and dry eye, needing careful management.

Recent genetic insights show that low-renin hypertension includes a range from essential hypertension to secondary or familial forms, affecting diagnosis and treatment.

A gene mutation causes woolly hair in a Syrian patient.

PCOS and related metabolic issues often run in families.

A boy had unusual synchronized hair growth with short active growth phases, not fitting known hair disorders.

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

Hormonal differences affect male pattern baldness.

Male pattern baldness is an unintended side effect of the body's use of androgens for muscle growth, especially in those genetically prone to it.

The clinical signs of Adams-Oliver syndrome can vary greatly, even among family members.

The document concludes that careful evaluation is key to diagnose and treat women with hair loss, with tests for thyroid, iron, and hormones as needed.

UK medical students lack dermatology education, liver biopsy patients with risk factors show more fibrosis, and certain fungi resist drugs due to melanin; genetics may influence female hair loss.

Researchers found new hair and nail genes, how hair reacts to UV, differences in white and pigmented hair growth, nerve changes in alopecia, treatments for baldness and alopecia, a toenail condition linked to a genetic disorder, and that nail fungus is more common in people with psoriasis.

The document concludes that AFA should be considered in patients with acromegaly-like features but normal hormone levels, and more cases need to be identified to understand the condition fully.

Hirsutism is excessive hair growth in women often caused by polycystic ovarian syndrome, and identifying the cause is important for managing associated health risks.

The Wnt signaling pathway is not a major factor in the development of keratoacanthoma, a type of skin tumor.

Hair microscopy is useful for diagnosing certain hair loss conditions but has limitations and must be interpreted carefully.

Keratosis pilaris is often linked to genetic mutations and causes skin and hair abnormalities, regardless of those mutations.

Kids with early graying hair often have low levels of calcium, ferritin, and vitamin D3.