PHENOTYPIC AND GENOTYPIC CHARACTERISTICS OF PROGRESSIVE FAMILIAL INTRAHEPATIC CHOLESTASIS TYPE 3 IN PEDIATRIC POPULATION IN PAKISTAN

نویسندگان

چکیده

OBJECTIVE: To determine the phenotypic and genotypic characteristics of progressive familial intrahepatic cholestasis (PFIC) type 3 in Pakistani children a hospital setting. METHODS: This cross-sectional observational study was conducted at department Pediatrics Gastroenterology & Hepatology, The Children’s Hospital Lahore, Pakistan from October 2020 to March 2021. Patients either sex under 16 years age presenting with jaundice, pruritus, neonatal or chronic liver gamma glutamyl transferase >100 IU/ml were included after taking informed consent by parents. For Molecular genetics 2ml blood EDTA sent an international laboratory free cost on research basis. Reports assessed levels noted genetic coding also recorded. Data entered analyzed SPSS version 22. data interpreted help clinical geneticist. RESULTS: Out 34 children, 14 (41.2%) males 20 (58.8%) females. Mean 6.71±3.10 years. Consanguinity 32 (94.1%) parents having positive family history 24 (70.6%) cases. most common mutation c. 1783C>T p.(Arg595*), 12 (35.3%) cases, followed 2861G>T p.(Gly954 ASP) [8 (23.5%) cases], 153G>A p.(Trp51) [3 (8.8%) 1714 C>T p.(Gln572*) 1906C>T p. (Gln636), 3220G>A p.(Gly1074Arg, 3433del (val1145Leufsx7) 2 (5.9%) cases each, 3859 p.(1287Argext*) 88-91del p.(Lys30gly fsx7) 1429c>T (Gln477) one (2.9%) case each. CONCLUSION: Children PFIC have variable presentation.

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Progressive familial intrahepatic cholestasis

Progressive familial intrahepatic cholestasis (PFIC) refers to a heterogeneous group of autosomal-recessive disorders of childhood that disrupt bile formation and present with cholestasis of hepatocellular origin. The exact prevalence remains unknown, but the estimated incidence varies between 1/50,000 and 1/100,000 births. Three types of PFIC have been identified and associated with mutations ...

متن کامل

Locus heterogeneity in progressive familial intrahepatic cholestasis.

Progressive familial intrahepatic cholestasis (PFIC or Byler disease) is a rare autosomal recessive form of severe and fatal cholestatic liver disease. A locus for PFIC has recently been mapped to chromosome 18q21-q22 in the original Byler pedigree. This region harbours the locus for a related phenotype, benign recurrent intrahepatic cholestasis (BRIC), suggesting that these traits are allelic....

متن کامل

Pancreatic adenocarcinoma in type 2 progressive familial intrahepatic cholestasis

BACKGROUND BSEP disease results from mutations in ABCB11, which encodes the bile salt export pump (BSEP). BSEP disease is associated with an increased risk of hepatobiliary cancer. CASE PRESENTATION A 36 year old woman with BSEP disease developed pancreatic adenocarcinoma at age 36. She had been treated with a biliary diversion at age 18. A 1.7 x 1.3 cm mass was detected in the pancreas on ab...

متن کامل

Genetic basis of progressive familial intrahepatic cholestasis.

oo~~ssrvn familial intrahepatic cholestasis (PFIC), P originally known as Byler disease, was first described in an Amish kindred (1,2). It is an inherited disorder of childhood in which cholestasis of hepatocellular origin often presents in the neonatal period or the first year of life and leads to death from liver failure at ages ranging from infancy to adolescence. Cholangiograms show normal ...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: Khyber Medical University Journal

سال: 2022

ISSN: ['2305-2643', '2305-2651']

DOI: https://doi.org/10.35845/kmuj.2022.21935