Antenatally diagnosed acrocallosal syndrome with intact corpus callosum: Second affected offspring [3]

Genetic Counseling

Volumn 16, Issue 4, 2005, Pages 425-428

  Tastekin, Ayhan ^a,b   Ingec, M ^a   Onbas, O ^a   Erdogan, F ^a   Ikbal, M ^a   Aydin, M D ^a   Ors, R ^a  

^a ATATURK UNIVERSITY   (Turkey)

^b ATATÜRK UNIVERSITY   (Turkey)

Author keywords

[No Author keywords available]

Indexed keywords

ACROCALLOSAL SYNDROME; ANAMNESIS; AUTOPSY; CASE REPORT; CLEFT LIP; CLINICAL FEATURE; CONSANGUINEOUS MARRIAGE; CORDOCENTESIS; CORPUS CALLOSUM AGENESIS; CRANIOFACIAL MALFORMATION; FETUS; FETUS ECHOGRAPHY; HUMAN; HYPERTELORISM; KARYOTYPE 46,XY; LETTER; LOW SET EAR; MALE; MICROPENIS; NUCLEAR MAGNETIC RESONANCE IMAGING; OMPHALOCELE; POLYDACTYLY; PRENATAL DIAGNOSIS; PRENATAL DRUG EXPOSURE; RADIATION EXPOSURE; SIBLING; SYNDACTYLY; AGENESIS; CORPUS CALLOSUM; FEMALE; GENE LOCATION; MEDICAL LITERATURE; MUSCLE HYPOTONIA; PREGNANCY TERMINATION; PROGENY; ULTRASOUND;

ABNORMALITIES, MULTIPLE; CORPUS CALLOSUM; CRANIOFACIAL ABNORMALITIES; FEMALE; HERNIA, UMBILICAL; HUMANS; INFANT, NEWBORN; MALE; PENIS; PREGNANCY; PRENATAL DIAGNOSIS; SYNDROME;

EID: 30444455893     PISSN: 10158146     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (5)

1. IKBAL M., TASTEKIN A., ORS R.: Micropenis in a newborn with acrocallosal syndrome. Genet. Counsel., 2004, 15(2), 233-235.
2. GELMAN-KOHAN Z., ANTONELLI J., ANKORI-COHEN H., ADAR H., CHEMKE J.: Further delineation of the acrocallosal syndrome. Eur. J. Pediatr., 1991, 150(11), 797-799.
3. CHRISTENSEN B., BLAAS H.G., ISAKSEN C.V., ROALD B., ORSTAVIK K.H.: Sibs with anencephaly, anophthalmia, clefts, omphalocele, and polydactyly: hydrolethalus or acrocallosal syndrome? Am. J. Med. Genet., 2000, 91(3), 231-234.
4. SCHINZEL A., KAUFMANN U.: The acrocallosal syndrome in sisters. Clin. Genet., 1986, 30(5), 399-405.
5. BIJARNIA S., BAIJAL A., VERMA I.C.: Genetic counseling in acrocallosal syndrome. Indian. J. Pediatr., 2003, 70(2), 169-171.