Journal of Developmental Medicine(Electronic Version)  2014, Vol. 2 Issue (2): 104-105 DOI: |
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| The Case Study of Alport Syndrome Family History and Eugenics Counseling |
PLA Family Planning, Prenatal and Postnatal Care Technology Research Institute People’s Liberation Amy No.202 Hospital Shenyang 110003 China
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Abstract [Abstract] Objects Analyze the genetic characteristic of Alport Syndrome (AS) to improve the quality of
genetic counseling. Method Investigated a family with family history of AS throughout four generations,
total 15 people. Result 7 people were diagnosed with AS, and 1 person was suspected patient. No one
throughout the four generations was married to relatives, but there were people showing AP symptom in three generations (no gender difference). Conclusion It is important to know how the AP gene was passed on through generations in the family, and its genetic characteristic. Patients should visit a doctor for prenatal diagnosis when it is necessary, so that the patient may only keep the healthy babies, in order to achieve the ecumenical purpose.
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Received: 13 February 2014
Published: 05 September 2019
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