🖼

Fig. 2 — Bi-allelic loss of function variants in SLC30A5 as cause of perinatal lethal car

active
paper figure Created: 2026-04-21T18:29:40 By: paper_figures_tool Quality: 50% 🔗 External ID: paper-fig-paper-556cd4824b5f-2
Fig. 2 — Bi-allelic loss of function variants in SLC30A5 as cause of perinatal lethal car
Fig. 2Figure 2
Imaging findings of the affected individuals. Prenatal ultrasound scans at the level of four-chamber view of individuals of family 1 ( A : Voluson S8, AB2-7 convex abdominal ultrasound transducer 2–8 MHz; B : Voluson E8, RAB 6-D convex abdominal transducer 2–8 MHz; C , D : Philips EPIQ Elite, V 2–7 convex abdominal ultrasound transducer 2–9 MHz): fetus 1.1 at 28 weeks of gestation ( A ) and fetus 1.3 at 31 weeks of gestation ( B ) showing edematous skin and lungs maximally compressed by massive pleural effusions, polyhydramnios. Prenatal myocardial hypertrophy in fetus 1.2 at 25 weeks of gestation ( C ) and in fetus 1.3 at 28 weeks of gestation ( D ). Postnatal ultrasound scans of individual 1.2 (Zonare ZS3, Mindray, USA): E spongy left ventricular myocardium (nonstandard plane nonstandard with 20 MHz linear transducer), F frontal hygroma in parasagittal view (blue crosses mark a distance of 1.2 cm, 7,5 MHz curved array transducer). G Postmortem babygram of individual 1.2 (bor
PubMed: paper-556cd4824b5f
Metadata
pmidpaper-556cd4824b5f
captionImaging findings of the affected individuals. Prenatal ultrasound scans at the level of four-chamber view of individuals of family 1 ( A : Voluson S8, AB2-7 convex abdominal ultrasound transducer 2–8 
image_urlhttps://www.ebi.ac.uk/europepmc/articles/PMC8110774/bin/41431_2020_803_Fig2_HTML.jpg
paper_titleBi-allelic loss of function variants in SLC30A5 as cause of perinatal lethal cardiomyopathy.
figure_labelFig. 2
figure_number2
_schema_version1
source_strategypmc_api
📊 Evidence Profile
Evidence Balance
+0%
Certainty
0%
Debates
0
Incoming
0
Outgoing
0
0 supporting 0 contradicting 0 neutral
View full evidence profile →
Public annotations (0)Annotate on Hypothes.is →
No public annotations yet.