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Keratosis Follicularis Spinulosa Decalvans is a rare genetic disorder causing skin and hair issues, often inherited through the X chromosome.

Longer GGN repeats in the androgen receptor gene are linked to polycystic ovary syndrome.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

Male pattern baldness is mostly inherited, involves many genes, and is linked to other traits like early puberty and strong bones.

The most different genetic segment between Africans and East Asians is the EDA2R/AR region, with two main types influenced by population changes and natural selection, and linked to baldness.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

Autism's genetics are linked with early age of puberty and less hair loss, but not with hormone levels or polycystic ovary syndrome.

Five new mutations in the androgen receptor gene were found, helping to understand androgen insensitivity syndrome better.

The document concludes that accurate diagnosis of ichthyosis is crucial for treatment and genetic advice, and ongoing research is needed for better therapies.

Protoporphyrin IX is useful in cancer treatment but can cause health problems if not properly regulated.

A subtle androgen receptor abnormality can allow normal male development and sometimes fertility despite partial androgen resistance.

The study found that males with KFSD had severe skin and eye symptoms, while female carriers had milder symptoms.

Steroid sulfatase is important for activating hormones that affect memory, brain function, and certain diseases, and could be a target for treating hormone-related disorders.

A rare genetic skin condition usually affecting males was found in a 9-year-old girl.

There's no significant genetic link between male pattern baldness and COVID-19.

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

New mutations in MBTPS2 reduce its function and cause IFAP syndrome with unusual symptoms.

A woman with CHILD syndrome showed skin abnormalities, and the report suggests CHILD nevus and NEVIL might be the same condition, highlighting the need for diagnosis for genetic advice.

Experts discussed treatments for skin conditions in children, emphasizing hydration, cautious medication use, and early intervention for infections.

The chapter explains that there are many genetic skin disorders affecting skin cell formation, including both common and rare types.

KFSD causes scarring hair loss and skin roughness, mainly in males.

The document concludes that specific hair and blood vessel abnormalities in infants with seizures and developmental issues may indicate Menkes disease, which lacks a cure and is often fatal by age 3.

An 18-year-old man was diagnosed with a rare genetic disorder causing hair loss, severe light sensitivity, and skin issues.

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

The conclusion is that adult males with muscle weakness and hormonal imbalances should be tested for Kennedy's disease.

A girl with a rare skin condition improved after one month of treatment with acitretin.

Kennedy's disease leads to muscle weakness and sensory issues, has no cure but manageable symptoms, and future treatments look promising.

Kennedy's disease leads to muscle weakness without a cure, but exercise and managing symptoms may help patients live a normal lifespan.

A new MBTPS2 gene variant disrupts fat metabolism and collagen production, causing Osteogenesis imperfecta.

The study concluded that key signs of Keratosis follicularis spinulosa decalvans are changes in terminal hair and vellus hair follicles, which likely start the inflammation and damage to hair follicles.