Search

everythinglearnresearchcommunity

for

Search:↓

Most cases were lichen planus pigmentosus, highlighting the need for accurate diagnosis for proper treatment.

Two boys had a rare skin condition needing to be differentiated from similar disorders, with unclear inheritance due to few cases.

People with Alopecia areata often have lower Vitamin D levels, which might affect the severity of their condition.

Treatment with vitamin A did not improve the child's skin condition.

Genetic changes in specific proteins contribute to hair loss in some women of African descent.

Genetic testing confirmed a rare disorder causing hair loss and vision problems in a Saudi family, stressing its importance for diagnosis and counseling.

Congenital Adrenal Hyperplasia is mainly caused by enzyme deficiencies, leading to varying symptoms like hormone imbalances and physical changes.

Iron deficiency can cause hair color changes, which can be reversed with iron supplements.

The patient has Chronic Cutaneous Lupus, a skin condition causing plaques and hair loss.

Certain mutations in the PADI3 gene may increase the risk of developing a type of scarring hair loss common in women of African descent.

Mutations in specific genes cause different types of ectodermal dysplasias.

Zinc deficiency can cause skin issues like hair loss and eczema.

Vitamin D deficiency is common in children with non-scarring alopecia, and managing it may help treatment.

Too much vitamin A can cause serious health problems.

Iron supplements can restore normal hair color in cases of premature graying linked to iron deficiency.

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

A man with hypoparathyroidism had other health issues that led to a diagnosis of a rare autoimmune disorder, APS-1.

Alopecia areata negatively affects family life, mental health, and quality of life in young people.

Malondialdehyde-modified DNA may trigger an immune response in alopecia areata patients.

Japanese patients with alopecia areata often have a higher BMI and consume more vitamin C, fruit, and retinol, which may affect their condition's development or severity.

Epigenetic changes in blood cells may contribute to alopecia areata.

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

Low levels of zinc and ferritin may worsen alopecia areata.

Folliculitis Decalvans and Frontal Fibrosing Alopecia can coexist in people with darker skin, showing features of both conditions.

Netherton syndrome in a boy caused skin and hair issues, and treatment didn't work.

Mutations in the KRT85 gene cause hair and nail problems.

Nail changes are common in alopecia areata and can indicate its severity.

KLB and EIF3C genes are key for early diagnosis of vitiligo and alopecia areata.

Zinc deficiency didn't cause visible hair changes in the patient.

No systemic causes were found for the patients' conditions.