15 more genetic variants connected to KCNK9 imprinting syndrome are found by researchers.

Chat Box 15 more genetic variants connected to KCNK9 imprinting syndrome are found by researchers.

[{"selector":"#anim-cf899753-bb59-437c-a661-fa0289a3c595 [data-leaf-element=\"true\"]","keyframes":{"transform":["translate3d(36.82025539447838%, 0, 0) translate(25%, 0%) scale(1.5)","translate3d(0%, 0, 0) translate(0%, 0%) scale(1)"]},"delay":500,"duration":4000,"easing":"cubic-bezier(.14,.34,.47,.9)","fill":"forwards"}] [{"selector":"#anim-714c7f5a-fde0-447f-9d71-c677f70851c2","keyframes":{"opacity":[1,1]},"delay":0,"duration":2000,"easing":"cubic-bezier(.3,0,.55,1)","fill":"both"}] [{"selector":"#anim-484e0dab-c8a9-4e3e-a856-3df6e1ac1af1","keyframes":{"transform":["scale(3)","scale(1)"]},"delay":0,"duration":2000,"easing":"cubic-bezier(.3,0,.55,1)","fill":"forwards"}] Chat Box The KCNK9 gene contains 15 other genetic abnormalities that result in a neurodevelopmental condition

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The disorder's symptoms can include intellectual incapacity, behavioural abnormalities,

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speech and movement impairments, and unusual facial traits.

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diagnosis as a result of the new study, which was reported in Genome Medicine.

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The lack of a specific treatment for KCNK9 imprinting syndrome

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Always suppressed is the father's gene.

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