Displaying publications 1 - 20 of 45 in total

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  1. Peng GP, Chuan YT
    Med J Malaysia, 1988 Jun;43(2):138-49.
    PMID: 3266287
    Matched MeSH terms: Congenital Abnormalities/mortality; Congenital Abnormalities/epidemiology*
  2. Highet HC
    Lancet, 1895;146:1605.
    DOI: 10.1016/S0140-6736(01)98823-3
    Matched MeSH terms: Congenital Abnormalities
  3. Ganesh Raj S, Norliza I, Mansharan Kaur CS
    JUMMEC, 2020;23(2):22-24.
    MyJurnal
    Congenital heart disease (CHD) is the result of a complicated interplay between genetic and non-genetic, or “environmental,” factors acting on the foetus and one of those environmental factors is maternal hyperglycemia. Maternal diabetes has teratogenic effects on the evolution of the foetal cardiovascular system; as a consequence, cardiovascular malformations are the most common anomalies in infants of diabetic mothers with transposition of the great arteries, tricuspid atresia and truncus arteriosus being some of the common cardiac malformations encountered. Thus, it is important to perform a detailed heart examination at autopsy of perinatal deaths in order to ascertain related anomalies. We present a case of stillbirth in a woman with Type 1 Diabetes mellitus on insulin therapy who claims she was unaware about her pregnancy.
    Matched MeSH terms: Congenital Abnormalities*
  4. Yap CK, Ismail A, Tan SG, Omar H
    Bull Environ Contam Toxicol, 2002 Dec;69(6):877-84.
    PMID: 12428166
    Matched MeSH terms: Congenital Abnormalities/etiology*; Congenital Abnormalities/veterinary*
  5. Sardharwalla IB, Lingam S, Harvey DR
    Arch Dis Child, 1988 Jun;63(6):672-3.
    PMID: 3389904
    Matched MeSH terms: Congenital Abnormalities/diagnosis; Congenital Abnormalities/prevention & control*
  6. Norlasiah IS, Clyde MM, Boo NY
    Med J Malaysia, 1995 Mar;50(1):52-8.
    PMID: 7752977
    During the period 1 January 1990-31 December 1990, 68 neonates with congenital abnormalities were successfully analysed for chromosome abnormalities in order to determine the contribution of chromosome aberrations to the aetiology of congenital abnormalities. The neonates were karyotyped employing the G-banding technique. Twenty-nine babies showed abnormal chromosome karyotypes. Twenty-six were observed to have classic trisomy syndromes; ie. trisomy 21 (32.3%), trisomy 18 (3.0%), and trisomy 13 (3.0%). The mean maternal age of the mothers with babies having normal karyotype was lower than the mean maternal age of the mothers having babies with abnormal karyotypes. From this study the incidence of congenital abnormalities due to chromosomal abnormalities is found to be 1:838 livebirths. Frequency of newborns having abnormal chromosomes is 0.14% for Malays, 0.12% for Chinese and 0.06% for Indians.
    Matched MeSH terms: Congenital Abnormalities/genetics*
  7. Tan DSK
    Med J Malaysia, 1983 Mar;38(1):15-8.
    PMID: 6633327
    The IgM-globulin levels were determined for 5,167 cord-sera of apparently normal infants and 281 sera of defective infants aged 4 months and younger. The significant level for IgM-globulin in neonates was found to be 20 mgm/dl (2 SD above mean of the normal) above which the level was regarded as abnormally raised. Significant levels of IgM-globulin were found in 0.2% (11/5, 167) ofnormal neonates and in 40.6% (114/281) of defective infants which is more than 200 times the normal value. Combining the normal and abnormal rates, an overall figure of 23 intrauterine infections per 1,000 live births were obtained for Malaysia. The advantages and disadvantages of the use of serum IgM-globulin elevations for the diagnosis of intrauterine infections were discussed.
    Matched MeSH terms: Congenital Abnormalities/blood*
  8. Leela Anthony, Nagarajah Lee, Stephen Ambu, Lokman Hakim S.
    MyJurnal
    This study examined the trend of major congenital anomalies (CA) in the state of Penang using the ICD 10 database from 1999 to 2004. The data was collected from various health centres and hospitals. The aim was to study the magnitude of the problem for congenital anomalies in the state of Penang in terms of trends and also to calculate the incidence rate by districts. If a trend was noticed, this in turn will determine whether to carry out further in-depth studies in the future and to find out the linkages to the environment if any.
    Matched MeSH terms: Congenital Abnormalities*
  9. HUTTER FH
    Med J Malaya, 1953 Dec;8(2):186-91.
    PMID: 13164689
    Matched MeSH terms: Congenital Abnormalities*
  10. Nik Mhd Nor NS, Ahmad Khairuddin SND, Ramli R
    BMJ Case Rep, 2024 Jan 09;17(1).
    PMID: 38199665 DOI: 10.1136/bcr-2023-259175
    Matched MeSH terms: Congenital Abnormalities*
  11. Reed JG
    Trans R Soc Trop Med Hyg, 1925;19:90-91.
    DOI: 10.1016/S0035-9203(25)80009-9
    Matched MeSH terms: Congenital Abnormalities
  12. Smith GH
    Lancet, 1841;37:358-359.
    DOI: 10.1016/S0140-6736(02)84452-X
    Matched MeSH terms: Congenital Abnormalities
  13. Boo NY
    Med J Malaysia, 2005 Oct;60(4):404-6.
    PMID: 16570699
    Matched MeSH terms: Congenital Abnormalities/prevention & control*
  14. Chakraborty R, Chakravarti A
    Hum Genet, 1977 Apr 07;36(1):47-54.
    PMID: 870410
    It has been reported that studies of the genetic consequences of inbreeding should adopt a different strategy in populations having a relatively old inbreeding history and where inbreeding levels have varied over time. This contention is tested with a series of 39,495 single-birth records from Bombay, India, collected in a World Health Organization survey on congenital malformations. Our analysis reveals that: 1. the incidence of major malformations is significantly higher among the inbred offspring (1.34%) as compared to that among non-inbred ones (0,81%)--a finding at variance with a previous study in the same area; 2. the inbreeding effect on perinatal mortality (stillbirths and mortality during the first few days of life) is also found to be significant. In view of the above findings, the genetic load as disclosed by inbreeding is computed for perinatal mortality, major malformations and pooling these together. A + B, the measure of the number of lethal equivalents per gamete, is found to be at variance with other reports. Such variability can be ascribed to non-genetic factors. Supporting evidence collected from Brazil and Malaysia in the same survey is also presented.
    Matched MeSH terms: Congenital Abnormalities/epidemiology
  15. Yew CW
    Med J Malaysia, 1977 Mar;31(3):232-5.
    PMID: 904518
    Matched MeSH terms: Congenital Abnormalities/diagnosis
  16. Cheah JS, Loh FK
    Med J Malaysia, 1973 Mar;27(3):217-9.
    PMID: 4268928
    Matched MeSH terms: Congenital Abnormalities/surgery
  17. Yaacob R, Zainal Mokhtar A, Abang Jamari DZH, Jaafar N
    BMJ Case Rep, 2017 Sep 23;2017.
    PMID: 28942402 DOI: 10.1136/bcr-2017-220801
    Fetus-in-fetu (FIF) is a rare entity in which malformed parasitic twin grows inside the body of its twin. It is most commonly presented with mass in the abdomen. We present a case of a 15-year-old boy who presented with abdominal mass since infancy. Radiological investigations are suggestive of FIF. Intraoperatively, malformed fetus in a sac was found and excised. Postoperatively the patient recovers well and was put on follow-up.
    Matched MeSH terms: Congenital Abnormalities/surgery
  18. Ng RL, Rajapathy K, Ishak Z
    Med J Malaysia, 2017 10;72(5):308-310.
    PMID: 29197888 MyJurnal
    Congenital arhinia is one of the rare craniofacial malformation that may cause severe respiratory distress at birth due to upper airway obstruction. Our patient, whose abnormalities were only detected after delivery in our centre, is the first reported case of congenital arhinia in Malaysia. Contrary to popular belief that neonates are obligate nasal breather, our patient adapted well to breathing through mouth before an elective tracheostomy was performed on day four of life.
    Matched MeSH terms: Congenital Abnormalities/physiopathology*
  19. Lee KW, Ching SM, Ramachandran V, Yee A, Hoo FK, Chia YC, et al.
    BMC Pregnancy Childbirth, 2018 Dec 14;18(1):494.
    PMID: 30547769 DOI: 10.1186/s12884-018-2131-4
    BACKGROUND: Gestational diabetes mellitus (GDM) is a of the major public health issues in Asia. The present study aimed to determine the prevalence of, and risk factors for GDM in Asia via a systematic review and meta-analysis.

    METHODS: We systematically searched PubMed, Ovid, Scopus and ScienceDirect for observational studies in Asia from inception to August 2017. We selected cross sectional studies reporting the prevalence and risk factors for GDM. A random effects model was used to estimate the pooled prevalence of GDM and odds ratio (OR) with 95% confidence interval (CI).

    RESULTS: Eighty-four studies with STROBE score ≥ 14 were included in our analysis. The pooled prevalence of GDM in Asia was 11.5% (95% CI 10.9-12.1). There was considerable heterogeneity (I2 > 95%) in the prevalence of GDM in Asia, which is likely due to differences in diagnostic criteria, screening methods and study setting. Meta-analysis demonstrated that the risk factors of GDM include history of previous GDM (OR 8.42, 95% CI 5.35-13.23); macrosomia (OR 4.41, 95% CI 3.09-6.31); and congenital anomalies (OR 4.25, 95% CI 1.52-11.88). Other risk factors include a BMI ≥25 kg/m2 (OR 3.27, 95% CI 2.81-3.80); pregnancy-induced hypertension (OR 3.20, 95% CI 2.19-4.68); family history of diabetes (OR 2.77, 2.22-3.47); history of stillbirth (OR 2.39, 95% CI 1.68-3.40); polycystic ovary syndrome (OR 2.33, 95% CI1.72-3.17); history of abortion (OR 2.25, 95% CI 1.54-3.29); age ≥ 25 (OR 2.17, 95% CI 1.96-2.41); multiparity ≥2 (OR 1.37, 95% CI 1.24-1.52); and history of preterm delivery (OR 1.93, 95% CI 1.21-3.07).

    CONCLUSION: We found a high prevalence of GDM among the Asian population. Asian women with common risk factors especially among those with history of previous GDM, congenital anomalies or macrosomia should receive additional attention from physician as high-risk cases for GDM in pregnancy.

    TRIAL REGISTRATION: PROSPERO (2017: CRD42017070104 ).

    Matched MeSH terms: Congenital Abnormalities/epidemiology*
  20. Daud AN, Bergman JE, Oktora MP, Kerstjens-Frederikse WS, Groen H, Bos JH, et al.
    PLoS One, 2017;12(3):e0173530.
    PMID: 28288183 DOI: 10.1371/journal.pone.0173530
    BACKGROUND: A number of transporter proteins are expressed in the placenta, and they facilitate the placental transfer of drugs. The inhibition of P-glycoprotein (P-gp) was previously found to be associated with an increase in the risk of congenital anomalies caused by drug substrates of this transporter. We now explore the role of other placental transporter proteins.

    METHODS: A population-based case-referent study was performed using cases with congenital anomalies (N = 5,131) from EUROCAT Northern Netherlands, a registry of congenital anomalies. The referent population (N = 31,055) was selected from the pregnancy IADB.nl, a pharmacy prescription database.

    RESULTS: Ten placental transporters known to have comparable expression levels in the placenta to that of P-gp, were selected in this study. In total, 147 drugs were identified to be substrates, inhibitors or inducers, of these transporters. Fifty-eight of these drugs were used by at least one mother in our cases or referent population, and 28 were used in both. The highest user rate was observed for the substrates of multidrug resistance-associated protein 1, mainly folic acid (6% of cases, 8% of referents), and breast cancer resistance protein, mainly nitrofurantoin (2.3% of cases, 2.9% of referents). In contrast to P-gp, drug interactions involving substrates of these transporters did not have a significant effect on the risk of congenital anomalies.

    CONCLUSIONS: Some of the drugs which are substrates or inhibitors of placental transporters were commonly used during pregnancy. No significant effect of transporter inhibition was found on fetal drug exposure, possibly due to a limited number of exposures.

    Matched MeSH terms: Congenital Abnormalities/metabolism*
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