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A new gene mutation causes vitamin D resistance and hair loss in two unrelated girls.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

An 8-year-old girl developed a rare skin condition in a linear pattern on one side of her body after a lung infection, which improved with treatment.

Four patients with a type of rickets and hair loss had different mutations in their vitamin D receptor gene, causing it to not work properly.

A COVID-19 infected patient with chronic kidney disease experienced worsened kidney function, hair loss, and unexpected wart clearance.

Too much IKZF1 and Ikaros protein may cause alopecia areata.

Genetic testing for EGFR mutations is crucial in similar cases.

The twins' condition is unique and doesn't match any known syndromes.

Certain gene variations are found in people with polycystic ovary syndrome.

Cannabidivarin (CBDV) may help brain cell growth and survival through the TRPV1 receptor.

Patients with the same vitamin D receptor mutation showed different symptoms due to other factors.

Lack of Vitamin D receptor changes skin structure and increases certain immune cells in the skin.

A child's rare skin disease was triggered by chickenpox.

Voriconazole can cause serious side effects, especially in long-term use.

HTLV-1-associated lichenoid dermatitis (HALD) is linked to an immune response against HTLV-1-infected cells.

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.

Skin issues are common in kids with chronic kidney disease.

New therapies like JAK inhibitors and stem cells show promise in treating vitiligo.

Relapsing hepatitis A can cause prolonged abnormal liver tests even without symptoms.

Early and accurate diagnosis is crucial for managing rare genetic disorders like this localized variant of junctional epidermolysis bullosa.

Quick diagnosis and biotin treatment can dramatically improve biotinidase deficiency symptoms.

Biotinidase deficiency can mimic other conditions, making early diagnosis and treatment crucial to prevent lasting issues.

Mice with a virus similar to COVID-19 had skin damage, but a special treatment helped repair it.

ADEM is a sudden brain disorder often following infection or vaccination, diagnosed by ruling out other conditions.

Tangent screens help detect visual field defects from vigabatrin.

Isolated rheumatic tricuspid valve disease is very rare.

Different skin conditions show distinct types of vessel inflammation, a new quality of life index for vulval disease is reliable, a certain intrauterine system might be linked to chronic vaginal yeast infections, and oral minoxidil reduces hair loss in women.

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