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Caudal Regression Syndrome


Drs Chillis, Farine, Morrow, Ritchie, Ryan; Lynn Salvador RDMS RDCS  01 January 2001   
Source: Platypus

 Summary  Ultrasound Features  Differential Diagnoses  Syndromes  Images 5  Show All 

Caudal regression syndrome represents a wide spectrum of malformations which ranges from imperforate anus to sirenomelia. It occurs during the third week of fetal development and is caused by a wedge-shaped defect in the posterior axis caudal blastema, causing malformation or fusion of the early lower limb buds. The different degrees of severity are related to different length and width of the early caudal defect.

Sirenomelia has been postulated as occurring in the presence of a single umbilical artery which diverts blood flow from the caudal portion of the embryo, producing malformation of caudal structures.

Caudal regression syndrome is more frequent in monozygotic twins and shows a 200-fold increase in diabetic mothers, occurring in 0.2 to 0.5 percent of these infants. The incidence is reported to be approximately one in 47,000 to 60,000 live births.

The syndrome includes distorted or absent vertebra below the thoracic level, rudimentary or absent pelvic bones and asymmetrically short lower limbs.

Associated malformations include gastrointestinal, genitourinary, and cardiac anomalies.Sonographic diagnosis of caudal regression syndrome has been reported from 17-34 weeks of pregnancy, and is frequently hindered by oligohydramnios. It has been suggested that the diagnosis of caudal regression syndrome includes lumbosacral agenesis of the spine, normal amniotic fluid volume and a three-vessel umbilical cord.

Sirenomelia may be diagnosed in the presence of oligohydramnios, bilateral renal agenesis, lower extremity fusion, and a two-vessel cord. Sirenomelia also involves absence of urinary, genital or anal orifices and no external genitalia although a tail or phallus may occasionally be found. Other genitourinary structures such as the bladder may also be missing. There may be missing kidneys or cystic dysplastic kidneys.

Amnioinfusion has been helpful in making a diagnosis in some cases with oligohydramnios.

Title: A case of partial sirenomelia and possible vitamin A teratogenesis
Author: von Lennep E, El Khazen N, De Pierreux G, Amy JJ, Rodesch F, Van Regemorter N
Journal: Prenatal Diagnosis 5: 35-40
Year: 1994

Title: In: Diagnostic Ultrasound of Fetal Anomalies: Text and Atlas
Author: Nyberg D, Mahony B, Pretorium D
Journal: Mosby Year Book: St. Louis, p187-191
Year: 1990

Title: In: Human Malformations and Related Anomalies Volume 2
Author: Stevenson R, Hall J, Goodman R
Journal: Oxford U Press: Oxford, p497
Year: 1993

Title: In utero diagnosis of caudal regression s
syndrome: report of three cases
Author: Loewry JA, Richards DG, and Toi A
Journal: J Clin Ultrasound 15: 469
Year: 1987

Title: Caudal regression syndrome: etiopathogenesis, prenatal diagnosis, and perinatal management
Author: Adra A, Cordero D, Mejides A, Yasin S, Salman F, O'Sullivan MJ
Journal: Ostet Gynecol 49, 508-516
Year: 1994

Title: In: Prenatal Diagnosis of Congenital Anomalies
Author: Romero R, Pilu G, Jeanty P, Ghidini A, Hobbins J
Journal: Appleton & Lange: Norwalk, p137
Year: 1988

Title: In: The Genetics of Renal Tract Disorders
Author: Crawfurd M d'A
Journal: Oxford University Press: New York/Oxford, p536-553
Year: 1988

Title: Multidisciplinary management of caudal regression syndrome (26 cases).
Author: Cama A, Palmieri A, Capra V, Piatelli GL, Ravegnani M, Fondelli P.
Journal: Eur J Pediatr Surg Dec;6 Suppl 1:44-5
Year: 1996

Title: Cryptorchidism as a caudal developmental field defect. A new description of cryptorchidism associated with
malformations and dysplasias of the kidneys, the ureters and the spi
Author: Cortes D, Thorup JM, Beck BL, Visfeldt J.
Journal: APMIS Oct;106(10):953-8
Year: 1998

Title: Caudal duplication syndrome.
Author: Dominguez R, Rott J, Castillo M, et al.
Journal: Am J Dis Child 147:1048-1052.
Year: 1993

Title: Abnormal anatomy of the lumbosacral region imaged by magnetic resonance in children with anorectal
malformations.
Author: Heij HA, Nievelstein RA, de Zwart I, Verbeeten BW, Valk J, Vos A.
Journal: Arch Dis Child May;74(5):441-4.
Year: 1996

Title: Caudal regression syndrome: MR appearance.
Author: Hirano H, Tomura N, Watarai J, Kato T.
Journal: Comput Med Imaging Graph Jan-Feb;22(1):73-6
Year: 1998

Title: Early detection of caudal regression syndrome: specific interest and findings in three cases.
Author: Subtil D, Cosson M, Houfflin V, Vaast P, Valat A, Puech F.
Journal: Eur J Obstet Gynecol Reprod Biol Sep;80(1):109-12
Year: 1998

Title: Segmental spinal dysgenesis: neuroradiologic findings with clinical and embryologic correlation.
Author: Tortori-Donati P, Fondelli MP, Rossi A, Raybaud CA, Cama A, Capra V.
Journal: AJNR Am J Neuroradiol Mar;20(3):445-56
Year: 1999

Title: Sirenomelia. Pathological features, antenatal ultrasonographic clues, and a review of current embryogenic
theories.
Author: Valenzano M, Paoletti R, Rossi A, Farinini D, Garlaschi G, Fulcheri E.
Journal: Hum Reprod Update Jan-Feb;5(1):82-6
Year: 1999


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