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Fig. 1 | BMC Medical Genomics

Fig. 1

From: Prenatal diagnosis identifies compound heterozygous variants in RYR1 that causes ultrasound abnormalities in a fetus

Fig. 1

A Pedigree of the non-consanguineous Chinese family. B–D Fetal II-5 ultrasound findings at 25 weeks of gestation showing the umbilical cord cysts. (B), abnormal conus medullaris morphology (C), and thickened heel subcutaneous tissue (D). E–K Fetal II-5 magnetic resonance imaging showing abnormality of the scrotum (E–F), thoracic scoliosis (G–H), abnormal conus medullaris morphology (I), hand clenching (J), and rocker bottom foot (K)

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BMC Medical Genomics

ISSN: 1755-8794

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