Brain anomalies associated with 47,XYY karyotypes detected on a prenatal scan [3]

Prenatal Diagnosis

Volumn 22, Issue 6, 2002, Pages 490-492

  Maymon, R ^a   Herman, A ^a   Reish, O ^a  

^a ASSAF HAROFEH MEDICAL CENTER   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

AUTOPSY; BLOOD SAMPLING; BRAIN MALFORMATION; CASE REPORT; CHROMOSOME MICRODISSECTION; CLINICAL FEATURE; DOWN SYNDROME; FETUS; GESTATIONAL AGE; HIGH RISK POPULATION; HUMAN; KARYOTYPE 47,XYY; LETTER; MALE; PHENOTYPE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; RISK ASSESSMENT; SEX RATIO;

ADULT; BRAIN; ECHOENCEPHALOGRAPHY; FEMALE; HUMANS; MALE; PREGNANCY; ULTRASONOGRAPHY, PRENATAL; XYY KARYOTYPE;

EID: 0036298462     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/pd.332     Document Type: Letter

References (11)

1. What parents are told after prenatal diagnosis of a sex chromosome abnormality: Interview and questionnaire study
2. First trimester transvaginal sonographic diagnosis of Dandy-Walker malformation
3. Cerebral malformations in the XYY syndrome
4. Prenatal decision following prenatal diagnosis of sex chromosome aneuploidy: A trend over time
5. Pneumoencephalographic and clinical findings of the XYY syndrome
6. Sex chromosomal anomalies in pregnancies conceived through intracytoplasmic sperm injection: A case for genetic counselling
7. Prenatal diagnosis of sex chromosome aneuploidy: Possible reasons for high rates of pregnancy termination
8. Maternal serum free beta- hCG and PAPP-A in fetal sex chromosome defects in the first trimester
9. Volumetric magnetic resonance imaging study of the brain in subjects with sex chromosome aneuploidies