Advances and Challenges in Prenatal Detection and Genetic Diagnosis of Upper Limb Anomalies: Analysis of a South London and Kent Cohort
Through a cross-sectional description of 188 cases with congenital upper limb anomalies, we discuss prenatal ultrasound detection (in terms of numbers and accuracy) and genetic diagnosis.
Authors
- Emma Fowler
- Colin Walsh (ORCID: https://orcid.org/0000-0003-4694-2805)
- Susan Bint
- Tessa Homfray (ORCID: https://orcid.org/0000-0002-9981-9678)
- Amira Elmakky (ORCID: https://orcid.org/0000-0002-9082-9490)
- L. Koutoulas
- Francesca Forzano (ORCID: https://orcid.org/0000-0001-5632-0052)
- Federica Ruscitti (ORCID: https://orcid.org/0000-0003-1857-7505)
- Muriel Holder‐Espinasse
- Tara Giacchino (ORCID: https://orcid.org/0000-0001-8434-6815)
- Ranjit Akolekar (ORCID: https://orcid.org/0000-0001-7265-5442)
- Lorenzo Garagnani (ORCID: https://orcid.org/0009-0002-7921-1371)
- Srividhya Sankaran
Institutions
- Canterbury Christ Church University (GB)
- Guy's Hospital (GB)
- St Thomas' Hospital (GB)
- King's College London (GB)
- Guy's and St Thomas' NHS Foundation Trust (GB)
- Medway NHS Foundation Trust (GB)
- St George's Hospital (GB)
- Harris Birthright Research Centre for Fetal Medicine (GB)
- King's College Hospital (GB)
- University of Genoa (IT)
Publication Details
- Journal
- Prenatal Diagnosis
- Published
- 2024-12-13
- DOI
- https://doi.org/10.1002/pd.6709
- Citations
- 2
- Primary Topic
- Congenital limb and hand anomalies
- Type
- article
- Field-Weighted Citation Impact
- 1.02