Download full-text PDF |
Source |
|---|---|
| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4050951 | PMC |
| http://dx.doi.org/10.4103/0019-5049.130845 | DOI Listing |
Publication Analysis
Top Keywords
Similar Publications
Covid-19 infection and vaccination during first trimester and risk of congenital anomalies: Nordic registry based study.
BMJ
July 2024
Department of Public Health, University of Copenhagen, Copenhagen, Denmark.
Objectives: To evaluate the risk of major congenital anomalies according to infection with or vaccination against covid-19 during the first trimester of pregnancy.
Design: Prospective Nordic registry based study.
Setting: Sweden, Denmark, and Norway.
Trichoscopic findings in neonatal alopecia in oro-facial-digital syndrome type 1.
Pediatr Dermatol
November 2024
Dermatology Department, Hospital Sant Joan de Déu, Universitat de Barcelona, Barcelona, Spain.
Article Synopsis
- - Oral-facial-digital syndrome type 1 (OFD1) is an X-linked dominant disorder caused by mutations in the OFD1 gene, resulting in various facial, oral, and digital abnormalities.
- - Skin symptoms occur in about 20%-30% of affected individuals and include evanescent milia (small cysts) and patchy hair loss (alopecia), which can mimic other conditions like tinea capitis.
- - Diagnosis can be confirmed through genetic testing, especially when clinicians suspect OFD1 due to specific trichoscopic findings, lack of response to antifungal treatments, and presence of midline anomalies.
Oro-facial-digital syndrome type 1 and neuronal migration disorders.
BMJ Case Rep
June 2024
Department of Microbiology, All India Institute of Medical Sciences, Bathinda, India.
Prevalence and associated factors of congenital anomalies in Ethiopia: A systematic review and meta-analysis.
PLoS One
April 2024
Department of Human Anatomy, School of Medicine, College of Health and Medical Sciences, Haramaya University, Harar, Oromia, Ethiopia.
Background: Congenital anomalies represent a significant contributor to infant mortality, morbidity, and enduring disability. With this in mind, the present investigation endeavour to ascertain the pooled prevalence of congenital anomalies and associated determinants among neonates in Ethiopia.
Method: PubMed, Google Scholar, CINAHAL, Hinari, and Global Health databases were systematically searched.
Updated EUROCAT guidelines for classification of cases with congenital anomalies.
Birth Defects Res
February 2024
Department of Paediatrics and Adolescent Medicine, Lillebaelt Hospital, University Hospital of Southern Denmark, Kolding, Denmark.
Background: Precise and correct classification of congenital anomalies is important in epidemiological studies, not only to classify according to etiology but also to group similar congenital anomalies together, to create homogeneous subgroups for surveillance and research. This paper presents the updated EUROCAT (European surveillance of congenital anomalies) subgroups of congenital anomalies and the updated multiple congenital anomaly (MCA) algorithm and provides the underlying arguments for the revisions.
Methods: The EUROCAT methodology is described.
Want AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!