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Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

Bimatoprost can cause longer, thicker, darker eyelashes and eyebrows.

The document concludes that Rabson-Mendenhall syndrome requires novel treatments for insulin resistance and emphasizes the importance of dental care in affected patients.

HNG may help prevent the negative effects of chemotherapy on sperm production and white blood cell counts.

A disease causing skin issues in young adult German short-haired pointers is hereditary, with most affected dogs not responding to treatment.

Review determines effective, safe treatments for female hair loss.

Review finds no permanent solution for female hair loss.

The report concludes that PCOS is mainly a condition of excess male hormones and its definition may change as new information is discovered.

Men with more vanadium in their blood and who drink less soy milk are more likely to have hair loss.

Get head MRI for babies with achondroplasia early, use free immunoglobulin light chains to detect certain neurodevelopmental disorders, and video calls work for speech therapy in patients with facial anomalies.

The most different genetic segment between Africans and East Asians is the EDA2R/AR region, with two main types influenced by population changes and natural selection, and linked to baldness.

The document concludes that PCOS in adolescents is complex and requires comprehensive care to manage its symptoms and associated health risks.

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

Best hair growth results from combining finasteride and minoxidil.

5% topical minoxidil improves hair density and quality in monilethrix patients.

A specific gene mutation (Y449H in K10) was found in a patient with severe skin disorder.

The gene for Clouston syndrome in a large Indian family is located in the 13q11-q12.1 region.

A mutation in the SREBF1 gene causes both hereditary mucoepithelial dysplasia and IFAP syndrome, which are related conditions.

Trichoscopy helped diagnose a teenage girl's hair loss as monilethrix.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

The enzyme RDH12 plays a role in vision and retinal disease, with mutations leading to early onset visual loss and blindness, but the exact disease mechanism is unclear and there are no treatments yet.

Birt–Hogg–Dubé syndrome is a rare genetic condition causing skin lesions, lung cysts, and a higher chance of kidney cancer.

A boy with Sjogren-Larsson syndrome has skin and muscle symptoms due to a specific enzyme deficiency.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

Nagashima-type palmoplantar keratosis in Asians is caused by a SERPINB7 gene mutation.

This is the first known case of parathyroid cancer in a patient with Birt Hogg Dube Syndrome.

Finasteride caused blisters on hands and feet.

A man with kidney tumors and lung cysts was diagnosed with Birt–Hogg–Dubé syndrome and treated successfully, with genetic testing confirming the diagnosis.

A 2-year-old girl had a hair disorder not shared by her identical twin.