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Spinal Muscular Atrophy (SMA) Carrier Testing

Spinal Muscular Atrophy (SMA) Carrier Testing

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概述
文件资料

An accurate and safe DNA testing to check if you are a carrier of Spinal Muscular Atrophy (SMA) and understand if you have a higher chance to have a child with that condition.

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概述

What is SMA?

SMA (Spinal Muscular Atrophy) is a neurological condition and a type of motor neuron disease which a person cannot control the movement of their muscles due to a loss of nerve cells in the spinal cord and brain stem. A person with SMA is unable to move, walk, eat or breathe without assistance.

 

What causes SMA?

SMA is caused by a mutation in the survival motor neuron gene 1 (SMN1 gene). Motor neurons are the nerve cells that control movement. Abnormal SMN1 gene leads to missing neuron protein critical for nerve function & muscle control.

 

Types of SMA

What is SMA Carrier?

SMA carrier is a person that has a mutant gene of SMA disease who usually does not display or show symptoms of the disease.

若父母亲同时为同一种疾病的带因者,小孩就可能同时遗传到双方的异常基因而患病,且隐性遗传病难以透过一般常规产前检测发现,因此常到了出生后才被发现异常。

If both parents are SMA carrier, there is a 25% risk that the offspring have the recessive trait in phenotype.

Expanded Carrier Screening适合对象:

  • Would like to understand their risk of having a child with SMA disease.
  • Have a family history of SMA disease.
  • 计划怀孕的夫妻/ 已怀孕的夫妻
  • 血缘关系较近的夫妻
  • 精卵捐赠者

Why choose GGA SMA Carrier Testing?

文件资料

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