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LARON SYNDROME


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CONGENITAL ADRENAL HYPERPLASIA
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Diabetes
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Duchenne Muscular Dystrophy
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Nephrotic Syndrome
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Osteogenesis Imperfecta
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Rheumatic Heart Disease
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Other

  • What is Laron Syndrome?
  • International Community Links
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Laron Syndrome - most commonly referred to as Growth Hormone Insensitivity (GHI) - is a rare genetic illness that affects children. When properly diagnosed Laron syndrome can be treated, but when left untreated, children fail to grow in stature, and their final adult height is significantly reduced. This has a very negative impact on their quality of life and fulfillment of their life potential.

Treatment cost can vary from US$700 to US$1,400, or more per month, per individual patient, with the duration of treatment lasting many years. Considering the economic inflation in Pakistan currently (an estimated 25% in a country whose GNI per capita is US$770 (UNICEF 2006)) the treatment for even well off families seems like a far-fetched dream.  

CLAN is proud to work with Laron syndrome communities around the world to drive change. Please click on the following flags to learn more about Laron syndrome in the following countries:​
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Pakistan
Click on the tabs above to access our rights flyers and additional resources.
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Acknowledgement of Country. In the spirit of reconciliation, CLAN acknowledges the Traditional Custodians of Country throughout Australia and the connections of Aboriginal and Torres Strait Islander peoples to land, sea and community. In particular, we acknowledge the Wallumedegal Peoples of the Eora Nation, on whose land CLAN (Caring & Living As Neighbours) is headquartered. We pay our respect to Elders past and present and extend that respect to all First Nations leaders around the world.

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  • Home
  • What We Do
    • About CLAN
    • Our Five Pillars
    • Child Rights >
      • CAH Rights Flyer
      • Diabetes Rights Flyer
      • Epilepsy Rights Flyer
      • RHD Rights Flyer
      • Asthma Rights Flyer
      • Childhood Cancer Rights Flyer
      • OI Rights Flyer
      • Newborn Screening Rights Flyer
    • Our Committee
    • Our Team >
      • CLAN Child Health Africa
      • CDOs
      • Youth Advisors
      • UN Youth Representatives
      • New Colombo Plan Scholarship Holders
      • Acknowledging people who have worked with CLAN
    • Partnerships
    • Policies >
      • Rights Protection and Inclusion
      • Participation, Empowerment and Local Inclusion
      • Sustainable Change
      • Quality and Effectiveness
      • Collaboration
      • Communication
      • Governance
      • Resource Management
      • People and Culture
  • Where We Work
    • WHO Africa Region >
      • Uganda
      • Burundi
      • Nigeria
      • Kenya
    • WHO Americas Region
    • WHO Eastern Mediterranean Region >
      • Pakistan
    • WHO Europe Region
    • WHO South-East Asia Region >
      • Indonesia
    • WHO Western Pacific Region >
      • Australia
      • Fiji
      • Philippines
      • Vietnam
  • Communities
    • Asthma
    • Autism
    • CAH
    • Cerebral Palsy
    • Childhood Cancer
    • Diabetes
    • DMD
    • Epilepsy
    • Nephrotic Syndrome
    • Nodding Syndrome
    • Osteogenesis Imperfecta
    • RHD
  • News
    • UN Events >
      • Commission on the Status of Women >
        • CSW70
        • CSW69
        • CSW 68
        • CSW67
      • Commission for Social Development >
        • CSocD64
        • CSocD62
      • Science Summit >
        • UNGA80 Science Summit
        • UNGA79 Science Summit
      • UN Youth Events >
        • Youth Voices for Health & Gender Equity
        • ECOSOC Youth Forum 2025
      • SIDS4
      • WHA 77
      • UNHLM on UHC
      • UNHLPF 2022 Report
    • MATES4Kids
    • IndigenousNCDs
    • COVID-19 >
      • COVID-19 Infographics
      • COVID-19 Resources >
        • Vaccines
    • Blogs
  • Donate
  • Fundraisers
    • Rare Disease Day 2022
    • CAH Awareness Month 2022
  • Contact