Choroid plexus cysts and oligohydramnios: Presenting echographic signs in a female fetus with deletion of the wolf-hirschhorn syndrome region (4p16.3)

Genetic Counseling

Volumn 12, Issue 4, 2001, Pages 387-388

  Witters, I ^a   Van Schoubroeck, D ^a   Fryns, J P ^a  

^a UNIVERSITY HOSPITALS LEUVEN   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; CASE REPORT; CHOROID PLEXUS TUMOR; CHROMOSOME 4P; CHROMOSOME DELETION 4; CYST; ECHOGRAPHY; FEMALE; FETUS; HUMAN; LETTER; OLIGOHYDRAMNIOS; WOLF HIRSCHHORN SYNDROME;

ADULT; CHOROID PLEXUS; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 4; CYSTS; FEMALE; FETAL DISEASES; HUMANS; KARYOTYPING; OLIGOHYDRAMNIOS; PREGNANCY; SYNDROME; ULTRASONOGRAPHY, PRENATAL;

CANIS;

EID: 0035680501     PISSN: 10158146     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (10)

1. Natural history of Wolf-Hirschhorn syndrome: Experience with 15 cases
2. Wolf-Hirschhorn syndrome (WHS): A history in pictures
3. De novo unbalanced translocation resulting in monosomy for proximal 14q and distal 4p in a fetus with intrauterine growth retardation Wolf-Hirschhorn syndrome, hypertrophic cardiomyopathy, and partial hemihypoplasia
4. Wolf-Hirschhorn syndrome with cryptic 4p16.3 deletion and balanced/unbalanced mosaicism in the mother
5. Amniotic fluid index measurements during pregnancy
6. The Wolf-Hirschhorn syndrome in fetuses
7. Wolf-Hirschhorn syndrome. Review of the literature and three case studies
8. Prenatal detection of congenital hypospadias in the Wolf-Hirschhorn (4p-) syndrome
9. Effect of the size of the deletion and clinical manifestation in Wolf- Hirschhorn syndrome: Analysis of 13 patients with a de novo deletion
10. Genotype-phenotype correlations and clinical diagnostic criteria in Wolf-Hirschhorn syndrome