Archive for the tag: rare

Customized Treatment For Rare Skin Disease Through Genetics

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For more information on dermatology or #YaleMedicine, visit: https://www.yalemedicine.org/stories/rare-skin-problems-treatment-genetics.

We hear a lot about treatments for skin problems like an acne flare-up, a worrisome mole, or eczema. But there are also quite a few rare, severe skin conditions that can have a major impact on quality of life, whether because they are painful or make you self-conscious about your appearance. Also, skin disorders can affect other parts of the body as well. For instance, erythrokeratodermia-cardiomyopathy (EKC) syndrome is a condition that causes plaques to form on the skin and also heart abnormalities. And people with genetic skin diseases are much more likely to experience depression. “Most disorders have a genetic basis, and in skin diseases, it’s incredibly easy to see them,” says dermatologist Keith Choate, MD, PhD. The unique thing about skin diseases, he says, is that the entire skin is made up of the same cells, performing different roles depending on the location on the body. “When we find a mutation in a new gene, the first thing that we do is ask, ‘What is the normal function of this gene within the skin?”’ Dr. Choate uses genetics to diagnose and treat rare skin diseases. At Yale, over a dozen new genetic skin diseases have been defined, and in some cases, Dr. Choate’s group has been able to develop treatments for them. ac
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Living with a rare skin disorder | The Skin We Wear | Full Episode

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**This documentary contains images that may be disturbing to some viewers. Viewer discretion is advised.**

Harlequin Ichthyosis is a rare genetic disorder that causes thick and scaly skin that is prone to cracking and constant infections. In the past, babies born with this condition rarely live beyond the first few days. Today, sufferers are able to lead normal and productive lives – but not without obstacles.

From 2-hour long oil baths and constant moisturising, to stares and judgement from strangers, their struggles are physical, social and emotional.

Enter the lives of four individuals coping with Harlequin Ichthyosis in Singapore, Hong Kong and Vietnam. Three-year-old Zoe may have lost all her hands due to the condition, but she’s not lost her joy for life. Despite being visibly different, 13-year-old Aliya navigates the teenage years with grace. Two-year-old Ngoc Bich is an orphan in Vietnam, waiting for a family to adopt her. And 26-year-old Mui Thomas’ achievements are proof that a fulfilling life is possible even with a lifelong condition.

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