2017-10-22  Case of the week # 458  © Lech Dudarewicz  www.TheFetus.net

---

Case of the week # 458

November 9, 2017 - November 23, 2017

 

Lech Dudarewicz, MD.



Case report

A young woman with unremarkable history was sent to our unit because of her husband was diagnosed with a genetic condition. The couple were advised about the 50% risk of the disease in offspring and scheduled for first trimester anomaly scan.
We obtained the following images in the first and second trimester:

Images 1 and 2.
 

 

Images 3-6.

  

Images 7-12.

 

  

Images 13-16.

  

Images 17.

Images 18 and 19.

Image 20.

When you have tried to solve the case on your own (no team work here please !) you can find the Answer here.

• Other items by Dudarewicz
• • Agenesis of the corpus callosum-HTML
    
  • Antiphospholipid syndrome and pregnancy-HTML
    
  • Arachnoid cyst, suprasellar-HTML
    
  • Asherman syndrome, uterine synechia-HTML
    
  • Autosomal recessive polycystic kidney disease-HTML
    
  • Campomelic dysplasia-HTML
    
  • Case of the week # 396 -Case
  • Case of the week # 400 -Case
  • Case of the week # 448 -Case
  • Cephalocele, occipital-HTML
    
  • Choledochal cyst-HTML
    
  • Coarctation of the aorta-HTML
    
  • Emanuel syndrome-HTML
    
  • Gastroschisis-HTML
    
  • Hemimelia, transverse-HTML
    
  • Holoprosencephaly, alobar-HTML
    
  • Holoprosencephaly, semilobar-HTML
    
  • Holoprosencephaly, semilobar versus hydrocephalus-HTML
    
  • Limb-body wall complex-HTML
    
  • Monosomy X,, edema of hands and feet -HTML
    
  • Osteogenesis imperfecta, type II-HTML
    
  • Parvovirus B19 infection, hydrocephalus -HTML
    
  • Persistent left superior vena cava-HTML
    
  • Persistent right umbilical vein-HTML
    
  • Pierre Robin anomalad-HTML
    
  • Right kidney agenesis with rudimentary ectopic kidney-HTML
    
  • Sacral agenesis-HTML
    
  • Single umbilical artery -HTML
    
  • Smith-Lemli-Opitz syndrome-HTML
    
  • Subamniotic hematoma presenting as a premature rupture of membranes -HTML
    
  • TRAP syndrome: case report and perspectives of prenatal therapy-HTML
    
  • Treacher Collins syndrome-HTML
    
  • Trisomy 13-HTML
    
  • Trisomy 18-HTML
    
  • Trisomy 18-HTML
    
  • Trisomy 21, absent nasal bones-HTML
    
  • Trisomy 21, complete atrioventricular septal defect in the first and second trimester -HTML
    
  • Trisomy 21, suspected atrioventricular canal -HTML
    
  • Wolf-Hirshorn syndrome-HTML