ultrasound diagnosis of fatal anomalies

PIERRE ROBIN SEQUENCE
Fig. 11.42 Pierre Robin sequence. Same fetus,
showing a three-dimensional scan of the fetal face.
board. Outreach committee consisting of
families available worldwide to correspond
via mail, phone, in person, or by e-mail.
Scope: National network
Founded: 1999
Address: P.O. Box 3274, Quincy, IL 62305,
United States
Telephone: 217–224–7480
Fax: 217–224–0292
E-mail: help@pierrerobin.org
Web: http://www.pierrerobin.org
References
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three-dimensional sonographic features of Pierre
Robin syndrome: case report. Gynecol Obstet Invest
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Megier P, Ayeva DM, Esperandieu O, Aubry MC, Couly G,
Desroches A. Prenatal ultrasonographic diagnosis of
the cerebro-costo-mandibular syndrome: case report
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Meizner I, Katz M, Bar ZJ, Insler V. Prenatal sonographic
detection of fetal facial malformations. Isr J Med Sci
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Morin G, Gekas J, Naepels P, et al. Cerebro-costo-mandibular
syndrome in a father and a female fetus:
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transmission. Prenat Diagn 2001;
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Pilu G, Romero R, Reece EA, Jeanty P, Hobbins JC. The
prenatal diagnosis of Robin anomalad. Am J Obstet
Gynecol 1986; 154: 630–2.
Rotten D, Levaillant JM, Martinez H, Ducou le Pointe H,
Vicaut E. The fetal mandible: a 2D and 3D sonographic
approach to the diagnosis of retrognathia
and micrognathia. Ultrasound Obstet Gynecol 2002;
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Soulier M, Sigaudy S, Chau C, Philip N. Prenatal diagnosis
of Pierre Robin sequence as part of Stickler syndrome.
Prenat Diagn 2002; 22: 567–8.
Winter RM, Crawfurd MA, Meire HB, Mitchell N.
Osteopathia striata with cranial sclerosis: highly
variable expression within a family including cleft
palate in two neonatal cases. Clin Genet 1980; 18:
462–74.
Fig. 11.43 Pierre Robin sequence. Photograph
taken after birth of the same fetus as in the previous
figure.
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