Familial occurrence of isolated Dandy-Walker variant in two consecutive male fetuses [2]

Genetic Counseling

Volumn 17, Issue 4, 2006, Pages 461-463

  Lin, Y H ^a   Chen, Chih Ping ^b,c,d   Chen, T C ^b   Liang, S J ^a   Hsu, C S ^a  

^a TAIPEI MEDICAL UNIVERSITY   (Taiwan)

^b MACKAY MEMORIAL HOSPITAL   (Taiwan)

^c ASIA UNIVERSITY   (Taiwan)

^d CHINA MEDICAL UNIVERSITY   (Taiwan)

Author keywords

[No Author keywords available]

Indexed keywords

AMNIOCENTESIS; ANAMNESIS; AUTOPSY; CASE REPORT; DANDY WALKER SYNDROME; FAMILIAL DISEASE; FEMALE; FETUS ECHOGRAPHY; FETUS KARYOTYPING; HUMAN; KARYOTYPE 46,XY; LETTER; MALE;

ABNORMALITIES, MULTIPLE; ABORTION, INDUCED; ANEUPLOIDY; CHROMOSOMES, HUMAN, PAIR 13; CHROMOSOMES, HUMAN, PAIR 18; CORPUS CALLOSUM; DANDY-WALKER SYNDROME; FEMALE; FETAL DISEASES; HUMANS; HYDROCEPHALUS; KARYOTYPING; PREGNANCY; TRISOMY; VARIATION (GENETICS);

EID: 33847246290     PISSN: 10158146     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (15)

1. BERNARD J.P., MOSCOSO G., RENIER D., VILLE Y.: Cystic malformations of the posterior fossa. Prenat. Diagn., 2001, 21, 1064-1069.
2. CARMEL P.W., ANTUNES J.L., HIALA S.K., GOLD A.T.: Dandy-Walker syndrome: clinicopathological features and reevaluation of the modes of treatment Surg. Neuro., 1977, 8, 132-138.
3. COWLES T., FURMAN P., WILKINS I.: Prenatal diagnosis of Dandy-Walker malformation in a family displaying X-linked inheritance. Prenat. Diagn., 1993, 13, 87-91.
4. ECKER J.L., SHIPP T.D., BROMLEY B., BENACERRAF B.: The sonographic diagnosis of Dandy-Walker and Dandy-Walker variant: associated findings and outcomes. Prenat. Diagn., 2000, 20, 328-332.
5. HIRSCH J.F., PIERRE-KAHN A., RENIER D., SAINTE-ROSE C., HOPPE-HIRSCH E.: The Dandy-Walker malformation. A review of 40 cases. J. Neurosurg., 1984, 61, 515-522.
6. KROES H.Y., NIEVELSTEIN R.J., BART P.G., NIKKELS P.G., BERGMANN C., GOOSKENS R.H., VISSER G., VAN AMSTEL H.K., BEEMER F.A.: Cerebral, cerebellar, and colobomatous anomalies in three related males: sex-linked inheritance in a newly recognized syndrome with features overlapping with Joubert syndrome. Am. J. Med Genet., 2005, 135A, 297-301.
7. LEHMAN R.M.: Dandy-Walker syndrome in consecutive siblings: familial hindbrain malformation. Neurosurg., 1981, 8, 717-719.
8. MURRAY J.C., JOHNSON J.A., BIRD T.D.: Dandy-Walker malformation: etiologic heterogeneity and empiric recurrence risks. Clin. Genet., 1985, 28, 272-283.
9. NYBERG D.A., MAHONY B.S., HEGGE F.N., JICKOK D., LUTHY D.A., KAPUR R.: Enlarged cisterna magna and the Dandy-Walker malformation: factors associated with chromosomal abnormalities. Obstet. Gynecol., 1991, 77, 436-442.
10. OBWEGESER R., DEUTINGER J., BERNASCHEK G.: Recurrent Dandy-Walker malformation. Arch. Gynecol. Obstet., 1994, 255, 161-163.
11. PETTIGREW A.L., JACKSON L.G., LEDBETTER D.H.: New X-linked mental retardation disorder with Dandy-Walker malformation, basal ganglia disease, and seizures. Am. J. Med. Genet., 1991, 38, 200-207.
12. PILU G., GOLDSTEIN I., REECE E.A., PEROLO A., FOSCHINI M.P., HOBBINS J.C., BOVICELLI L.: Sonography of fetal Dandy-Walker malformation: a reappraisal. Ultrasound. Obstet. Gynecol., 1992, 2, 151-157.
13. RUSS P.D., PRETORIUS D.H., JOHNSON M.J.: Dandy-Walker syndrome, a review of 15 cases evaluated by prenatal sonography. Am. J. Obstet. Gynecol., 1989, 161, 401-406.
14. ULM B., ULM M.R., DEUTINGER J., BERNASCHEK G.: Isolated Dandy-Walker malformation: prenatal diagnosis in two consecutive pregnancies. Am. J. Perinatol., 1999, 16, 61-63.
15. WAKELING E.L., JOLLY M., FISK N.M., GANNON C., HOLDER S.E.: X-linked inheritance of Dandy-Walker variant. Clin. Dysmorphol., 2002, 11, 15-18.