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10.1002/mgg3.902

Jalili syndrome (JS) is a rare cone‐rod dystrophy (CRD) associated with amelogenesis imperfecta (AI).

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10.3390/ijms20246279

CNNM4 is abundant in the brain and the intestinal tract, and its abnormal activity causes Jalili Syndrome.

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10.3390/ijms20051135

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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10.1136/jmedgenet-2018-105716

Jalili syndrome is a rare genetic disorder first identified by Jalili in Gaza.

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10.29252/qums.13.8.73

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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Jalili Syndrome

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Aug 16, 2022

What is/are Jalili Syndrome?

Jalili Syndrome - Jalili syndrome (JS) is a rare cone‐rod dystrophy (CRD) associated with amelogenesis imperfecta (AI). ^[1] CNNM4 is abundant in the brain and the intestinal tract, and its abnormal activity causes Jalili Syndrome. ^[2] 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. ^[3] Jalili syndrome is a rare genetic disorder first identified by Jalili in Gaza. ^[4] 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. ^[5]