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A boy with GAPO syndrome had hair loss similar to male pattern baldness without hormone issues, possibly due to skin or blood vessel problems.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

Three new types of a skin blistering disease were found, caused by specific gene mutations.

CAH is a genetic disorder affecting cortisol production and causing hormonal imbalances, with treatment and diagnosis varying by form and symptoms.

A girl with Netherton syndrome was able to eat wheat without allergies after a special treatment.

Three siblings with a genetic form of rickets showed different symptoms of the disease.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

A child with rickets and hair loss might have a rare type of rickets that doesn't improve much with usual vitamin D and calcium treatment.

Two siblings with a rare type of rickets and hair loss had low vitamin D levels, which is not typical for their condition.

The document describes a rare case of IFAP syndrome, a genetic condition with symptoms of hair loss, light sensitivity, and scaly skin.

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

A child with a rare type of rickets showed some improvement with high doses of vitamin D, but such conditions often respond poorly to treatment.

The document concludes that patient outcomes for Congenital Adrenal Hyperplasia are often not ideal because of poor management and a need for better diagnosis and treatment methods.

Netherton Syndrome is a non-treatable genetic disorder in children causing skin, hair, and allergy issues.

Pregnancies in a woman with the Donohue mutation were managed with genetic testing, resulting in three healthy infants.

Congenital Adrenal Hyperplasia is a genetic disorder with two forms, causing symptoms like early puberty and severe acne, but can be identified through screening and treated with glucocorticoids.

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.

Antifungal treatment can improve severe skin infections with cutaneous horns.

A rare skin condition causes red and dark patches on the face and limbs.

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.

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

A mutation in the FAM83G gene is linked to skin and hair abnormalities in two related individuals.