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Creatinin i.u. 0.21 g/l 036-1.30
STOFFWECHSELLABOR/NEUROBLASTOM
organische sauren i.u.
the organic acids in this urine show an elevated
4-HYDROXYPHENYLLACTIC ACID(86.7 mmol/mol creatinine
normalL 3.1).DICARBOXYLIC ACIDS(ADIPID SUBERIC SEBACIC)
were also detected.
This pattern may be only a child with some liver damage
who was fed with mideium chain fatty acids a fw days
before.
It may also suggest a patient with ZELLWGER or a similar
peroxisomal disease.
The DICARBOXYLIC ACIDS may also suggest a BETAOXIDATION
DEFECT.
If the symptoms of child correspond to ZELLWEGER
SYNDROME please send Plasma or Serum for the eterination
of VKLCFA.
It is frequently very difficult to interpretet the resulty
of the ORGANIC ACID ANALYSIS without any clinical
information on the child.

اینم جواب ازمایش ادراری که به المان فرستاده شد.

بچه ها باورتون نمیشه!  برای بچم از «داستان من» با اسم و عکس خودش کتاب سفارش دادم، امروز رسید خیلی جذذذابه، شما هم برید ببینید، خوندن همه کتابها با اسم بچه خودتون مجانیه، کودکتون قهرمان داستان میشه، اینجا میتونید مجانی بخونید و سفارش بدید.

ازمایشگاه نیلو چی شد؟؟؟؟؟؟؟؟؟؟؟؟؟؟؟؟؟؟؟؟؟؟؟؟؟

به نظر شما ایا امکان داره در بارداری بعدی چنین مشکلی پیش بیاد؟؟؟؟؟؟؟؟؟؟؟؟؟؟؟؟؟؟؟؟؟؟؟؟؟؟؟
کمکم کنید لطفا

منتظر راهنماییتون هستم
فاطی عزیز،

1- علت اصلی Neonatal Giant Cell Hepatitis فقدان کامل غده هیپوفیز می باشد. ولی در بسیاری از موارد هنوز علت آن ناشناخته است (ایدیوپایتک)
2- شما را به مطالعه مقالات ذیل دعوت می کنم:
www.nature.com/jp/journal/v22/n3/full/7210670a.html
www.ncbi.nlm.nih.gov/pmc/articles/PMC503066
medical-dictionary.thefreedictionary.com/Giant+Cell+Hepatitis
journals.lww.com/.../Neonatal_Giant_Cell_Hepatitis__Histological_and.13.aspx
www.clinicaladvances.com/article_pdfs/gh-article-200907-khan.pdf
www.nejm.org/doi/full/10.1056/NEJM199207093270218
فاطی عزیز،
1) What is Neonatal Hepatitis?

Neonatal hepatitis is inflammation of the liver that occurs only in early infancy, usually between one and two months after birth. About 20 percent of the infants with neonatal hepatitis are infected by a virus that caused the inflammation before birth by their mother or shortly after birth. These include cytomegalovirus, rubella (measles), and hepatitis A, B or C viruses. In the remaining 80 percent of the cases no specific virus can be identified as the cause, but many experts suspect that a virus is to blame.
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2) What are the Symptoms and how is it Diagnosed?

The infant with neonatal hepatitis usually has jaundice (yellow eyes and skin), that appear at one to two months of age, is not gaining weight and growing normally, and has an enlarged liver and spleen. The infant cannot absorb vitamins for proper growth.

The jaundice is caused by the childs bile ducts becoming inflamed and enlarged, blocking the flow of bile into the small intestine for digestion of fats and absorption of vitamins. This results in the yellow pigment of bile seeping into the blood stream, causing the yellowing of the skin and eyes. In the 80 percent of the cases where there is no virus identified as the cause, a liver biopsy is performed, where a small piece of the liver is taken out of the child with a needle and examined with a microscope.

The biopsy will often show that four or five liver cells are combined into a large cell that still functions, but not as well as a normal liver cell. This type of neonatal hepatitis is sometimes called "giant cell hepatitis."

The symptoms of neonatal hepatitis are similar to another infant liver disease, biliary atresia, in which the bile ducts are destroyed for reasons that are not understood. The infant with biliary atresia is also jaundiced and has an enlarged liver, but is growing well and does not have an enlarged spleen. These symptoms, along with a liver biopsy and blood tests, are needed to distinguish biliary atresia from neonatal hepatitis.
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3) What are the Complications?

Patients with neonatal hepatitis caused by rubella or cytomegalovirus are at risk of developing an infection of the brain that could lead to mental retardation or cerebral palsy. Many of these infants will also have permanent liver disease from the destruction of liver cells and the resulting scarring (cirrhosis).

Infants with giant cell hepatitis usually recover (80 percent of cases) with little or no scarring to their liver. Their growth pattern resumes as bile flows normally into the small intestine for digestion and to absorb vitamins.

About 20 percent of the infants with neonatal giant cell hepatitis develop chronic liver disease and cirrhosis. Their liver becomes very hard, due to the scarring, and the jaundice does not disappear by six months of age. Infants who reach this point in the disease eventually will require a liver transplant.

Because of the blockage of the bile ducts and the damage caused to liver cells, infants with chronic neonatal hepatitis will not be able to digest fats and will not be able to absorb vitamins A, D, E and K. The lack of vitamin D leads to poor bone and cartilage development (rickets). Vitamin A is also needed for normal growth and good vision. Vitamin K deficiency is associated with easy bruising and a tendency to bleed, whereas the lack of vitamin E results in poor coordination.

Chronic neonatal hepatitis will lead to the inability of the liver to eliminate toxins in the bile. This causes itching, skin eruptions and irritability.
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4) How is Neonatal Hepatitis Treated?

There is no specific treatment for neonatal hepatitis. Vitamin supplements are usually prescribed and many infants are given phenobarbital, a drug used to control seizures, but which also stimulates the liver to excrete additional bile. Formulas containing more easily digested fats are also given to the infant.

Neonatal hepatitis caused by the hepatitis A virus also usually resolves itself within six months, but cases that are the result of infection with the hepatitis B or hepatitis C viruses most likely will result in chronic liver disease. Infants who develop cirrhosis ultimately will need a liver transplant.
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5) Can Neonatal Hepatitis be Spread to Others?

Infants with neonatal hepatitis caused by the cytomegalovirus, rubella or the hepatitis A, B, and C viruses may transmit the infection to others who come in close contact with the infant.

These infected infants should not come into contact with pregnant women because of the possibility that the woman will transmit the virus to her unborn child.
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باسلام وخسته نباشید
من در هفته 30 بارداری هستم.هفته 27 سونوگرافی شدم .دکتر سونوگرافی گفتند مایع بطن راست مغز جنین کمه.سونورو به دکترم نشون دادم گفتند اصلا مهم نیست تو جنین پسر شایع هستش بدنیا بیاد خوب میشه.
میخواستم بونم نظر شما چی هستش.
با تشکر
آزمایشگاه نیلو جان

من هفته 14 بارداری هستم سنو که رفتم گفتش که حجم هر دو تخمدان بدون توده فضاگیر بوده و بزرگتر از حد معمولی می باشد (8 تا 10 cc )خیلی نگرانم ایا مشکلی واسه نی نی نداره در ضمن من چون تنبلی تخمدان داشتم با دارو های تحریک کننده باردار شدم به نظرتون این میتونه یه دلیل باشه برای بزرگ شده تخمدان
سلام آقای آزمایشگاه نیلو
من هفته 14 بارداری هستم. در هفته 13 سونوگرافی انجام دادم برای NT =0.7 بوده و NB=3.5 گفتند که نرماله دکترم برای تست غربالگری هفته 16 رو نوشته می خواستم بدونم از زنجان کدوم آزمایشگاهها نمونه رو برای شما می فرستند و کدومشون مطمئنتره؟
به نظرتون برای آزمایش لازمه بیام تهران؟
سلام خسته نباشید من در هفته 10 بارداری آزمایش خون دادم که بعضی نتایجش این بود:
wbc:9500
lymphocyte:21
netropill:76
mch:25/57
mchc:31/71
دکترم گفت خوبه ولی یکم از نرمال کمتر بود.الان سوالم اینه که این کم بودنش نشونه عفونت در خون هست؟الانم گلوم درد نمیکنه ولی خیلی خیلی خشک هست وسوزش داره-به نظرتون مشکلی هست لازمه دوباره آزمایش خون بدم ببینم عفونت در خون دارم یا نه؟
سلام آزمایشگاه نیلو عزیز
من 34 سال و ده ماه هستم و هفته 17 و دو روز بارداری می باشم. هفته 12 و چهار روز در آزمایشگاه نیلو غربالگری سه ماهه اول را انجام دادم . نتایج آن به صورت زیر است:
NT=1 MM NASAL BONE=PRESENT
FBHCG=48.00 (MoM=1.45)
PAPP-A=2743(MoM=0.86)
T21 PRIOR RISK=1:411 T18 PRIOR RISK=1:4577 T13 PRIOR RISK=1:11842
TRISOMY 21= 1:5192 TRISOMY 18<1:30000 TRISOMY 13<1:30000

در هفته 16 و دو روز در آزمایشگاه تخت طاووس (توصیه پزشک) غربالگری سه ماهه دوم را انجام دادم . نتایج آن به صورت زیر است:
AFP=22.2 (MoM=0.72) Ue3=1.54 (MoM=0.54) Hcg=39000(MoM=1.42)
DIA=290.7(MoM=1.60)
OSB=1:40500
DOWN SYNDROM=1:59 AGE ALONE=1:407 EQUIVALENT AGE RISK=42.9
TRISOMY 18=1:8800
هنوز جواب را به پزشکم نشان ندادم.اما بسیار نگران هستم.چرا در آزمایش اول علیرغم دقت بالاتر ریسک سندرم داون نداشت اما در سه ماهه دوم 43 درصد ریسک دارم. به نظر شما باید آزمایش را تکرار کنم و حتی آمینو سنتز بدم؟خودم برای اطمینان بیشتر ترجیح می دهم دوباره در آزمایشگاه نیلو آزمایش بدهم.
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