Recurrent fetal syndromic spina bifida associated with 3q26.1-qter duplication and 5p13.33-pter deletion due to familial balanced rearrangement
Objective: Neural tube defects belong to the second most common group of congenital anomalies, after heart defects, which can be diagnosed by prenatal ultrasonography. Rarely, neural tube defects can be associated with chromosomal abnormalities, including full and partial aneuploidies. We report a f...
Saved in:
Main Authors: | Egle Preiksaitiene (Author), Eglė Benušienė (Author), Zivile Ciuladaite (Author), Vytautas Šliužas (Author), Violeta Mikštienė (Author), Vaidutis Kučinskas (Author) |
---|---|
Format: | Book |
Published: |
Elsevier,
2016-06-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
A novel CHD7 variant disrupting acceptor splice site in a patient with mild features of CHARGE syndrome: a case report
by: Evelina Siavrienė, et al.
Published: (2019) -
Subtelomeric study of 132 patients with mental retardation reveals 9 chromosomal anomalies and contributes to the delineation of submicroscopic deletions of 1pter, 2qter, 4pter, 5qter and 9qter
by: Tommerup Niels, et al.
Published: (2005) -
Spina bifida and myelomeningocoele
by: Michael Katzen
Published: (1969) -
Spina Bifida and Carbamazepine
by: J Gordon Millichap
Published: (1991) -
Malignant melanoma and spina bifida
by: Sarah O'Mahony, et al.
Published: (2024)