Prenatal sonographic diagnosis of Aarskog syndrome

Journal of Ultrasound in Medicine

Volumn 18, Issue 10, 1999, Pages 707-710

  Sepulveda, Waldo ^a,b   Dezerega, Victor ^a   Horvath, Eleonora ^a   Aracena, Mariana ^a  

^a HOSPITAL DR SÓTERO DEL RÍO   (Chile)

^b CLÍNICA LAS CONDES   (Chile)

Author keywords

[No Author keywords available]

Indexed keywords

AARSKOG SYNDROME; ADULT; ARTICLE; CASE REPORT; FEMALE; FETUS; FETUS ECHOGRAPHY; HIGH RISK PREGNANCY; HUMAN; PRENATAL DIAGNOSIS; X CHROMOSOME LINKED DISORDER;

EID: 0032829912     PISSN: 02784297     EISSN: None     Source Type: Journal    
DOI: 10.7863/jum.1999.18.10.707     Document Type: Article

References (12)

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3. Teebi AS, Rucquoi JK, Meyn MS: Aarskog syndrome: Report of a family with review and discussion of nosology. Am J Med Genet 46:501, 1993
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7. Grier RE, Farrington FH, Kendig R, et al: Autosomal dominant inheritance of the Aarskog syndrome. Am J Med Genet 15:39, 1983
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10. Porteous MEM, Curtis A, Lindsay S, et al: The gene for Aarskog syndrome is located between DXS255 and DXS566 (X11.2-Xq13). Genomics 14:298, 1992
11. Glover TW, Verga V, Rafael J, et al: Translocation break-point in Aarskog syndrome maps to Xp11.21 between ALAS2 and DXS323. Hum Mol Genet 2:1717, 1993
12. Pasteris NG, Cadle A, Logie LJ, et al: Isolation and characterization of the faciogenital dysplasia (Aarskog-Scott syndrome) gene: A putative Rho/Rac guanine nucleotide exchange factor. Cell 79:669, 1994