Recurrence of complex camptopolydactyly in a sibling suggestive of autosomal recessive mode of inheritance [1]

American Journal of Medical Genetics

Volumn 116, Issue 1, 2003, Pages 94-96

  Phadke, Shubha R ^a   Agarwal, Savita ^a   Puri, Ratna Dua ^a  

^a SANJAY GANDHI POSTGRADUATE INSTITUTE OF MEDICAL SCIENCES   (India)

Author keywords

[No Author keywords available]

Indexed keywords

AUTOSOMAL RECESSIVE INHERITANCE; CAMPTODACTYLY; HAND MALFORMATION; HUMAN; LETTER; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; SIBLING;

ABORTION, EUGENIC; CONSANGUINITY; FATAL OUTCOME; FEMALE; FETAL DEATH; GENES, RECESSIVE; HAND DEFORMITIES, CONGENITAL; HUMANS; MALE; POLYDACTYLY; PREGNANCY; SIBLINGS; ULTRASONOGRAPHY, PRENATAL;

EID: 0037214261     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (4)

1. Benacerraf B, Miller W, Frigoletto F. 1988. Sonographic detection of fetuses with trisomies 13 and 18: Accuracy and limitations. Am J Obstet Gynecol 158:404-409.
2. Bromley B, Benacerraf B. 1995. Abnormalities of hands and feet in the fetus: Sonographic findings. Am J Roentgenol 165:1239-1243.
3. Bromley B, Shipp TD, Benacerraf B. 2000. Isolated polydactyly: prenatal diagnosis and perinatal outcome. Prenatal Diag 20:905-908.
4. Phadke SR, Gautam P. 1999. Complex camptopolydactyly: An unusual hand malformation. Am J Med Genet 83:191-192.