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The Lanceolate hair-J mutation in mice mimics human hair disorders like Netherton's syndrome.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

Hair transplants are effective for some women and many male-to-female transgender patients if done carefully by an experienced team.

CaBP1 and 2 are necessary for maintaining calcium currents and hearing in inner ear cells.

An infant with complete hair loss was diagnosed with a genetic disorder affecting hair growth.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

Melanoma risk tools need improvement, a gene mutation causes a hair disorder that might be treated by managing cell stress, a potential therapy for a skin-ear disorder involves blocking cell channels, skin wrinkling may indicate lung aging regardless of smoking, and oxidative stress might contribute to common baldness.

Melanoma risk tools need improvement, certain gene mutations cause skin diseases and could be treated by targeting those mutations, skin wrinkling may relate to lung aging due to genetic factors, and oxidative stress affects hair loss but can be reduced in low oxygen.

The absence of functional sebaceous glands causes hair follicle destruction and scarring alopecia.

Minoxidil can improve hair growth in some patients with woolly hair due to LIPH variants, with varying responses and mild side effects.

The study concluded that PKP1 is essential for skin integrity and hair growth, and its dysfunction causes the symptoms of ectodermal dysplasia/skin fragility syndrome.

With careful management, people with congenital adrenal hyperplasia can have successful pregnancies and become parents.

Estrogen and prolactin may play bigger roles in female hair loss than previously thought.

Caffeine may help hair growth in hereditary hair loss.

A patient with Werner syndrome showed a range of aging-like symptoms and metabolic issues, underscoring the need for early detection and treatment.

Netherton Syndrome can cause severe skin lesions in rare cases.

The document suggests treating individuals with nonclassic congenital adrenal hyperplasia who show symptoms, especially those related to excess male hormones.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Mutations in the PTPRQ gene cause significant balance issues in mice due to hair bundle defects in the inner ear.

Non-classic congenital adrenal hyperplasia is a common disorder causing symptoms like acne and infertility, and it's managed based on symptoms, not just test results. Treatment can improve fertility and reduce miscarriage risk.

Oral minoxidil shows promise in treating monilethrix-related hair loss.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

Mice with CBS deficiency are healthier on a low-methionine diet.

Methionine restriction works better than betaine for treating CBS deficiency symptoms in mice.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

Patients with Shwachman-Diamond syndrome often get misdiagnosed due to a wide range of symptoms, including immune system problems and bone abnormalities.

Dihydrotestosterone treatment can help penis growth in boys with 5α-reductase deficiency but doesn't fully normalize size after puberty.

Mutation in hairless gene may increase hair loss risk.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

Women with nonclassic 21-hydroxylase deficiency can have successful pregnancies through IVF, with certain factors affecting their chances.