E-ISSN 1658-8088 | ISSN 1658-807X
 

Original Article
Online Published: 15 Nov 2020
 


Knowledge and attitudes regarding etiology and genetic counseling among Saudi children with primary congenital glaucoma

Abdulwahab AlThib, Rajiv Khandekar, Deepak Edward.


Abstract
Background: Primary prevention of primary congenital glaucoma (PCG) includes improving families of children with PGC. We evaluated the level of knowledge and attitudes of parents of children on PCG in Saudi Arabia.
Methodology: This was a personal interview-based survey of parents of children with PCG at a tertiary eye hospital in Saudi Arabia. The study was conducted in 2018. A close-ended questionnaire in Arabic was used. Demographic data were collected on the children and parents. Clinical data on PCG were collected from electronic case records. Five questions each on knowledge and attitudes toward genetic counseling were queried. A Likert-type scale was used to collect the responses. Rasch analysis was carried out for knowledge and attitudes. The score was correlated with demographics and clinical determinants. p < 0.05 was considered statistically significant.
Results: The study sample comprised 60 participants. The median Rasch score for knowledge on genetic counseling for PCG was -4.57 [interquartile range (IQR) -7.28; -1.0]. The median Rasch score for attitudes toward genetic counseling for PCG was -8.9 (IQR -11.6: -5.9). Parents with more than one family member with PCG had a significantly higher knowledge than those with one family member with PCG (p = 0.007). Knowledge of
etiology and genetic counseling was significantly better if the child had residual vision amenable to low vision care (p < 0.001). The Rasch scores for knowledge and attitude were positively correlated (p < 0.001).
Conclusion: Knowledge of the cause of PCG and genetic counseling was high among parents. The positive attitude toward genetic counseling could be useful for the primary prevention of CG in Saudi Arabia.

Key words: Primary congenital glaucoma, genetic counseling, prevention, etiology, birth defects


 
ARTICLE TOOLS
Abstract
PDF Fulltext
How to cite this articleHow to cite this article
Citation Tools
Related Records
 Articles by Abdulwahab AlThib
Articles by Rajiv Khandekar
Articles by Deepak Edward
on Google
on Google Scholar


How to Cite this Article
Pubmed Style

AlThib A, Khandekar R, Edward D. Knowledge and attitudes regarding etiology and genetic counseling among Saudi children with primary congenital glaucoma. JBCGenetics. 2021; 4(1): 22-26. doi:10.24911/JBCGenetics/183-1599478278


Web Style

AlThib A, Khandekar R, Edward D. Knowledge and attitudes regarding etiology and genetic counseling among Saudi children with primary congenital glaucoma. https://www.jbcgenetics.com/?mno=132458 [Access: November 14, 2024]. doi:10.24911/JBCGenetics/183-1599478278


AMA (American Medical Association) Style

AlThib A, Khandekar R, Edward D. Knowledge and attitudes regarding etiology and genetic counseling among Saudi children with primary congenital glaucoma. JBCGenetics. 2021; 4(1): 22-26. doi:10.24911/JBCGenetics/183-1599478278



Vancouver/ICMJE Style

AlThib A, Khandekar R, Edward D. Knowledge and attitudes regarding etiology and genetic counseling among Saudi children with primary congenital glaucoma. JBCGenetics. (2021), [cited November 14, 2024]; 4(1): 22-26. doi:10.24911/JBCGenetics/183-1599478278



Harvard Style

AlThib, A., Khandekar, . R. & Edward, . D. (2021) Knowledge and attitudes regarding etiology and genetic counseling among Saudi children with primary congenital glaucoma. JBCGenetics, 4 (1), 22-26. doi:10.24911/JBCGenetics/183-1599478278



Turabian Style

AlThib, Abdulwahab, Rajiv Khandekar, and Deepak Edward. 2021. Knowledge and attitudes regarding etiology and genetic counseling among Saudi children with primary congenital glaucoma. Journal of Biochemical and Clinical Genetics, 4 (1), 22-26. doi:10.24911/JBCGenetics/183-1599478278



Chicago Style

AlThib, Abdulwahab, Rajiv Khandekar, and Deepak Edward. "Knowledge and attitudes regarding etiology and genetic counseling among Saudi children with primary congenital glaucoma." Journal of Biochemical and Clinical Genetics 4 (2021), 22-26. doi:10.24911/JBCGenetics/183-1599478278



MLA (The Modern Language Association) Style

AlThib, Abdulwahab, Rajiv Khandekar, and Deepak Edward. "Knowledge and attitudes regarding etiology and genetic counseling among Saudi children with primary congenital glaucoma." Journal of Biochemical and Clinical Genetics 4.1 (2021), 22-26. Print. doi:10.24911/JBCGenetics/183-1599478278



APA (American Psychological Association) Style

AlThib, A., Khandekar, . R. & Edward, . D. (2021) Knowledge and attitudes regarding etiology and genetic counseling among Saudi children with primary congenital glaucoma. Journal of Biochemical and Clinical Genetics, 4 (1), 22-26. doi:10.24911/JBCGenetics/183-1599478278





Most Viewed Articles
Most Accessed Articles

  • Frontonasal dysplasia: a review
    Muhammad Umair, Farooq Ahmad, Muhammad Bilal, Muhammad Arshad
    JBCGenetics. 2018; 1(2): 66-76
    » Abstract » doi: 10.24911/JBCGenetics/183-1530765389

  • The role of C-terminal tensin-like (Cten) gene in cancer metastasis
    Saleh Alghamdi, Sarah Alkwai, Mohammad Ilyas
    JBCGenetics. 2018; 1(1): 2-9
    » Abstract » doi: 10.24911/JBCGenetics/183-1531548689

  • Clinical reassessment of post-laboratory variant call format (VCF) files
    Lamia Alsubaie, Saeed Alturki, Ali Alothaim, Ahmed Alfares
    JBCGenetics. 2018; 1(1): 31-36
    » Abstract » doi: 10.24911/JBCGenetics/183-1529928114

  • Microcephalic osteodysplastic primordial dwarfism type II and Klinefelter syndrome: report of two competing growth syndromes
    AlAnoud Al-Jarbou, Afnan Al-Turki, Suha Tashkandi, Eissa A. Faqeih
    JBCGenetics. 2018; 1(1): 37-39
    » Abstract » doi: 10.24911/JBCGenetics/183-1530040885

  • Recessive ARFGEF2 mutation causes progressive microcephaly, epilepsy, and a distinct MRI pattern
    Maram Alojair, Abdulaziz Alghamdi, Kalthoum Tlili, Sateesh Maddirevula, Fowzan Sami Alkuraya, Brahim Tabarki
    JBCGenetics. 2018; 1(1): 40-42
    » Abstract » doi: 10.24911/JBCGenetics/183-1531469195

  • Most Downloaded
    Top Downloaded Articles

  • Frontonasal dysplasia: a review
    Muhammad Umair, Farooq Ahmad, Muhammad Bilal, Muhammad Arshad
    JBCGenetics. 2018; 1(2): 66-76
    » Abstract » doi: 10.24911/JBCGenetics/183-1530765389

  • Generation of a mouse model of Primary Hyperoxaluria Type 1 via CRISPR/Cas9 mediated gene editing
    Kimberly A Coughlan, Rajanikanth J Maganti, Andrea Frassetto, Christine M DeAntonis, meredith Wolfrom, Anne-Renee Graham, Shawn M Hillier, Steven Fortucci, Hoor Al Jandal, Sue-Jean Hong, Paloma H Giangrande, Paolo GV Martini,
    JBCGenetics. 2019; 2(1): 28-39
    » Abstract » doi: 10.24911/JBCGenetics/183-1542047633

  • Syndactyly genes and classification: a mini review
    Muhammad Umair, Farooq Ahmad, Muhammad Bilal, Safdar Abbas
    JBCGenetics. 2018; 1(1): 10-18
    » Abstract » doi: 10.24911/JBCGenetics/183-1532177257

  • Recessive ARFGEF2 mutation causes progressive microcephaly, epilepsy, and a distinct MRI pattern
    Maram Alojair, Abdulaziz Alghamdi, Kalthoum Tlili, Sateesh Maddirevula, Fowzan Sami Alkuraya, Brahim Tabarki
    JBCGenetics. 2018; 1(1): 40-42
    » Abstract » doi: 10.24911/JBCGenetics/183-1531469195

  • Consanguinity, awareness, and genetic disorders among female university students in Riyadh, Saudi Arabia
    Hadil Alahdal, Huda Alshanbari, Hana Saud Almazroa, Sarah Majed Alayesh, Alaa Mohammad Alrhaili, Nora Alqubi, Fai Fahad Alzamil, Reem Albassam
    JBCGenetics. 2021; 4(1): 27-34
    » Abstract » doi: 10.24911/JBCGenetics/183-1601264923

  • Most Cited Articles
    Most Cited Articles

  • Frontonasal dysplasia: a review
    Muhammad Umair, Farooq Ahmad, Muhammad Bilal, Muhammad Arshad
    JBCGenetics. 2018; 1(2): 66-76
    » Abstract » doi: 10.24911/JBCGenetics/183-1530765389
    Cited : 4 times [Click to see citing articles]

  • Syndactyly genes and classification: a mini review
    Muhammad Umair, Farooq Ahmad, Muhammad Bilal, Safdar Abbas
    JBCGenetics. 2018; 1(1): 10-18
    » Abstract » doi: 10.24911/JBCGenetics/183-1532177257
    Cited : 4 times [Click to see citing articles]

  • Genomics in Saudi Arabia Call for Data-Sharing Policy
    Ahmed Alfares,
    JBCGenetics. 2018; 1(2): 51-52
    » Abstract » doi: 10.24911/JBCGenetics/183-1546945268
    Cited : 4 times [Click to see citing articles]

  • Consanguinity, awareness, and genetic disorders among female university students in Riyadh, Saudi Arabia
    Hadil Alahdal, Huda Alshanbari, Hana Saud Almazroa, Sarah Majed Alayesh, Alaa Mohammad Alrhaili, Nora Alqubi, Fai Fahad Alzamil, Reem Albassam
    JBCGenetics. 2021; 4(1): 27-34
    » Abstract » doi: 10.24911/JBCGenetics/183-1601264923
    Cited : 2 times [Click to see citing articles]

  • Harel-Yoon syndrome: the first case report from Saudi Arabia
    Alaa AlAyed, Manar A. Samman, Abdul Ali Peer-Zada, Mohammed Almannai
    JBCGenetics. 2020; 3(1): 22-27
    » Abstract » doi: 10.24911/JBCGenetics/183-1585816398
    Cited : 2 times [Click to see citing articles]