readx;

When I watched it, the sentence that impressed me the most was that there are two kinds of people in this world, one is those who are relied on by others, and the other is those who rely on others. Pen × fun × Pavilion www. ｂｉｑｕｇｅ。 ｉｎｆｏ

And I'm undoubtedly the kind of person who is relied upon.

Relied on by his parents, relied on by his wife, and relied on by his young master.

This month, the young master has made a lot of progress, weight and height because of the daily growth hormone, has been improving, recently, because of the increase in leg strength, he can occasionally use his abdomen to climb forward, and even put a TV on the sofa, the young master can still lie on the sofa, stand and watch for a while.

For him, that's a good step forward.

But I still can't be happy.

At the end of July, my wife and I checked the young master's genes and did chromosomal screening. Just some time ago, the results came out.

What is the conclusion?

The sample had a heterozygous mutation in the COL11A1 gene associated with Hall syndrome and Stickler syndrome type 2, and the pedigree verification results were obtained from his father. At the same time, there was a semizygous mutation in the genes related to neonatal severe encephalopathy, X-linked mental retardation syndrome type 13 and rett syndrome, and the family verification results came from the mother.

If dominant inheritance is followed, if the patient and the father have similar symptoms, the heterozygous mutation may cause the disease, and if the father is asymptomatic, it is theoretically not pathogenic. If the recessive inheritance law is followed, it is theoretically a carrier and does not cause disease.

Theoretically, semizygous, homozygous, and compound heterozygous mutations may cause disease, and the mutation in this patient has a slightly higher carrier rate in the population, because the source of the mother, if it follows the dominant inheritance law, it may theoretically be pathogenic, and whether the disease in women is related to the X chromosome. If the recessive inheritance law is followed, the hemizygous mutation of the MECP2 gene may theoretically cause disease.

There are a lot of sprinkles, and the final conclusion is that if my wife and I have another child and a boy, it is very likely that we will repeat the mistakes of the past and become the same as the young master, a cerebral palsy. And if you give birth to a girl, maybe God willing, you can be safe and sound.

When I heard the news, I gave up on having a second child, because unless I was planning a divorce, I had to risk that my wife and I's next child would be a girl.

Otherwise, if it was a boy, then his fate would be the same as Zhao Wenxuan.

This month, my updates are not good, my subscriptions are not good, and my family affairs are not going well, as if everything is back to that time, that dark day.

Now my only hope is that the young master can learn to take care of himself, so that even if one day I am gone, he can live.

Son, come on!

I didn't want to post a single chapter, but I found that the word count was a bit too much, and if I didn't send a single chapter, many people would misunderstand me.

To be honest, I feel really uncomfortable, but there is nowhere else to talk to it, I can only say it in the book, if you don't like it, you can just take the book off the shelves.