Anales de la Facultad de Medicina
ISSN 1025-5583 versión impresa
HUERTAS, Erasmo, INGAR, Jaime, GUTIERREZ, Guiselle et al. Síndrome de costillas cortas y polidactilia: displasia esquelética fetal incompatible con la vida. An. Fac. med., ene./mar. 2010, vol.71, no.1, p.46-46. ISSN 1025-5583.
Short rib-polydactyly syndrome is a descriptive category for a group of lethal skeletal dysplasias characterized by hypoplastic thorax, short ribs, short limbs, polydactyly, and visceral abnormalities. The 4 established variants are SRPS I (Saldino-Noonan type), SRPS II (Majewski type; 263520), SRPS III (Verma-Naumoff type; 263510), and SRPS IV (Beemer-Langer type; 269860). All variants are thought to be inherited in autosomal recessive pattern. Because of the frequent phenotype overlap there is controversy as to whether the variants are due to variable expression or to genetic heterogeneity. We present a case of a male fetus, with typical ultrasound markers of skeletal dysplasia such as micromelia, bell shaped narrow thorax, hypertelorism, low implantation ears and polidactily who was born by vaginal delivery and died two days later due to respiratory insufficiency present since birth.
Palabras llave: Short rib-polydactyly syndrome; bone diseases, developmental; ultrasonography.
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