Autopsy, radiographic, and prental ultrasonographic examination of a stillborn fetus with femoral facial syndrome

American Journal of Medical Genetics

Volumn 71, Issue 1, 1997, Pages 76-79

  Urban, Jill E ^a,b   Mamus, Ronald M ^a,b   Stanaard, Michael W ^a,b   Sogers, Beverly Barton ^a,b  

^a UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER   (United States)

^b CHILDREN S MEDICAL CENTER   (United States)

Author keywords

Autopsy; Femoral facial syndrome; Femoral hypoplasia unusual faci s syndrome; Histology; Radiographs; Ultrasound

Indexed keywords

ARTICLE; BONE GROWTH; CARTILAGE CELL; CLEFT PALATE; FACE MALFORMATION; FEMOROFACIAL SYNDROME; FEMUR; FETUS; FETUS ECHOGRAPHY; HUMAN; HUMAN TISSUE; MATERNAL DIABETES MELLITUS; MICROGNATHIA; PRIORITY JOURNAL; STILLBIRTH; UROGENITAL TRACT MALFORMATION; VERTEBRA MALFORMATION;

ADULT; AUTOPSY; CLEFT PALATE; DIABETES, GESTATIONAL; FACE; FEMALE; FEMUR; FETAL DEATH; HUMANS; MALE; PREGNANCY; SPINE; SYNDROME; ULTRASONOGRAPHY, PRENATAL;

EID: 0030953699     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: None     Document Type: Article

References (13)

1. Burn J, Winter JB, Baraitser M, Hall CM, Fixsen J (1984): The femoral iiypopiasia-unusuai fades syndrome. J Med Genet 21:331-340.
2. naetl DL, Smith DVv, Scott C>, Hall BD, Gooding CA (1975): Femoral hypoplasia-unusual faciès syndrome. J Pediatr 86:107-111.
3. DePalma L, Duray PH, Popeo VR ; 19861: Femoral hypuplasia-unusual facies syndrome: Auicpsy findings in an unasual case. Pedialr Pathol 5:1-8.
4. Grix A (1982): Malformations in infants of diabetic mothers. Am J Med Genet 13:131-137.
5. Johnson JP, Carey JC, Gooch WM, Petersen J, Beattie JF (1983): Femoral hypopidsia-unusual faciès syndrome in infants of diabetic mothers. J Pcdiatr 102:866-872.
6. Lampert HP ;1980): Dominant inheritance of femora] hypoplasia-unusual fades syndrome. Clin Genet 17:2,r>5-258.
7. Lord J, Beighton P (1981): The femorai hypoplasia-unusual facies syndrome: A genetic entity? Clinical Genet 20:267-275.
8. Opitz JM (1993): Blastogenesis and ihe primary fieid in human development. Birth Defects OAS 29:3-37.
9. Opitz JM, Czeizel A, Evans JA. Hall JG, Lubinsky MS, Spranger JW (1987): NosoiOgic groupings in birth defects, in Vogei F, Sperling K (eds): Human Genetics. Proceedings of VII International Congress on Human Genetics, Berlin. Heidelberg: Springer-Verlag, pp 382-385.
10. Pitt DB, Findlay II, Cole WG, Rogers JG (1982): Case report: Femoral hypopiasia-unusuai faciès syndrome. Austral Paediatr J 18:63-66.
11. Kobinow, M, Sonek J, Buttino L, Veghte A (19951: Femoral-facial syndrome-Prenatal diagnosis-autosomal dominant inheritance. Am J Med Genet 57:397-399.
12. Sparnon AL, Ahmed S (1984): Urologicaî anomalies in the caudal regression syndrome. Austral NZ J Sm'g 54:365-367.
13. Tadmor OP, Mannerman C, Rabinowitz R, Fisher D, Itzchaki M, Aboulafia Y, Diamant YZ (1S93): Femoral hypoplasia-unusual faciès syndrome: Prenatal ultrasonographic observations. Fetal Diagn Ther 8:279-284.