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Diagnosing both systemic lupus and hemoglobinopathy is challenging due to overlapping symptoms.

The symposium highlighted the importance of understanding disease mechanisms for targeted dermatology treatments.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

A cross-bred lamb with severe skin and movement issues had ichthyosis fetalis but normal vitamin A levels.

A Saudi individual initially identified as a girl had a genetic disorder affecting gender development.

A 27-year-old with APS-1 showed improvement in symptoms after treatment.

Doctors should consider Netherton syndrome in patients with chronic skin and hair issues to avoid misdiagnosis.

A baby with maple syrup urine disease improved from skin problems by adjusting his diet to correct amino acid levels.

Genetic testing confirmed a rare skin disorder in a young girl, which improved with zinc supplementation.

An infant with a zinc deficiency skin disorder improved with zinc treatment.

A 5-year-old Akita with a rare skin condition improved significantly after treatment.

A patient with sickle cell trait and low vitamin D might have lupus, a rare combination that needs more attention.

Children with classic congenital adrenal hyperplasia have thicker heart fat and more heart and blood vessel risk factors, especially if their condition is not well-controlled.

Bovines can have rare inherited skin diseases with specific symptoms like hair loss, fragile skin, and abnormal porphyrin buildup.

Hormones, especially testosterone and DHT, are key for penis development and function, and testosterone therapy may help with erectile dysfunction in those with low levels.

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

Gene mutations can cause problems in male genital development.

Vitamin D3 and its receptor are important for hair growth, and understanding receptors could help treat hair graying and skin cancer.

Marie-Unna Hereditary Hypotrichosis is a rare genetic condition causing sparse hair growth, requiring specific recognition for proper care.

A 72-year-old man was diagnosed with a rare skin form of Rosai-Dorfman disease after years of misdiagnosis.

Mimicking growth factors in a topical solution can prolong hair growth phase and reduce hair loss without side effects.

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.

A woman's nail separation was likely caused by poor blood flow, and a treatment for similar conditions might help.

Surgery on a baby with a skin disorder improved eyelid position and eye health.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

Nonclassic congenital adrenal hyperplasia is a common genetic disorder that can cause a range of symptoms and requires personalized treatment.

Transverse sections are better for non-scarring hair loss, vertical sections are better for lichen planopilaris, and either method works for other scarring hair loss types.

Mutations in the P2RY5 gene cause hereditary woolly hair.

Finasteride significantly increases scalp hair and prevents hair loss in young and middle-aged men.

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