Introduction to Jalili Syndrome
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Jalili syndrome (JS) is a rare cone‐rod dystrophy (CRD) associated with amelogenesis imperfecta (AI).
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CNNM4 is abundant in the brain and the intestinal tract, and its abnormal activity causes Jalili Syndrome.
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The human family includes four members, whose impaired activity causes diseases such as Jalili Syndrome or Familial Hypomagnesemia, but is also linked to neuropathologic disorders, altered blood pressure, and infertility.
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Jalili syndrome is a rare genetic disorder first identified by Jalili in Gaza.
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Received: 28 Nov, 2018 Accepted: 27 Aug, 2019 Background and Objectives: Jalili syndrome is a rare autosomal recessive genetic disorder, which so far, only 33 families with this disorder have been reported worldwide.
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