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Bovines can have rare inherited skin diseases with specific symptoms like hair loss, fragile skin, and abnormal porphyrin buildup.

Loose Anagen Hair Syndrome is a hereditary condition causing hair loss in children due to abnormal hair follicles.

Some families have a genetic condition where they are born with irregular scalp defects.

Eruptive vellus hair cysts are a cosmetic skin condition, more common in young adults, with few effective treatments.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

Two siblings were the first reported cases of inheriting both eye coloboma and loose anagen syndrome together.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

A boy and his father with hereditary hypotrichosis simplex were treated for hair loss, but the treatment result is unknown.

Tigason improved hair growth in a boy with monilethrix without side effects.

The document discusses various eye conditions and their treatments, including a rare eye cancer in a baby, vision loss from a cancer drug, cataracts from a baldness treatment, a rare skin disorder, and a specific type of eye disease diagnosed with a special imaging technique.

The document explains how to identify different hair problems using a microscope.

Epidermolytic ichthyosis can be inherited in a semidominant way with mild symptoms in carriers.

Monilethrix is a rare genetic hair disorder that's hard to treat.

Birt–Hogg–Dubé syndrome is a rare genetic condition causing skin lesions, lung cysts, and a higher chance of kidney cancer.

Scientists used stem cells to create a model of the skin disease Epidermolysis Bullosa simplex, which helped them understand its molecular mechanisms and could aid in finding treatments.

The TRPV3 gene variant may cause the long-haired suri alpaca coat.

The man has a genetic skin condition called pachyonychia congenita.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

Two siblings were found to have a genetic condition causing progressive hair loss and woolly hair, which may often be misdiagnosed.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

The cornified envelope is crucial for skin's barrier function and involves key proteins and genetic factors.

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

A boy with a rare form of early puberty caused by a new gene mutation responded well to treatment aimed at reducing testosterone and preserving adult height.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

Pattern baldness is likely caused by a dominant gene influenced by testosterone levels, making it more common in men.

Hair shaft dysplasias are abnormal hair conditions that can be inherited or acquired and may signal other health issues, with limited treatment options available.