The Catel-Manzke syndrome in a female infant

Genetic Counseling

Volumn 9, Issue 3, 1998, Pages 187-190

  Kant, S G ^a   Oudshoorn, A ^a   Tjon Pian Gi, C V ^b   Zonderland, H M ^a   Van Haeringen, A ^a  

^a LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

^b GROENE HART HOSPITAL   (Netherlands)

Author keywords

Catel Manzke syndrome; Dysmorphic syndrome; Hand malformations

Indexed keywords

ARTICLE; CASE REPORT; CATEL MANZKE SYNDROME; CLEFT PALATE; CLINICAL FEATURE; CONGENITAL MALFORMATION; FEMALE; FINGER MALFORMATION; HUMAN; INDEX FINGER; INHERITANCE; MICROGNATHIA; NEWBORN; SEX RATIO;

ABNORMALITIES, MULTIPLE; CLEFT PALATE; FEMALE; FINGERS; HEART DEFECTS, CONGENITAL; HUMANS; INFANT, NEWBORN; METACARPUS; SYNDROME;

EID: 0031727197     PISSN: 10158146     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (20)

1. BERND L., MARTINI A.K. and SCHILTENWOLF M.: Catel-Manzke syndrome. Klin. Padiatr., 1990, 202, 60-63.
2. BRUDE E.: Pierre Robin sequence and hyperphalangy - a genetic entity (Catel- Manzke syndrome). Eur. J. Pediatr., 1984, 142, 222-223.
3. CATEL W.: Differentialdiagnose von Krankheitssymptomen bei Kindern und Jugendlichen. Vol , 3rd ed. Stuttgart, Thieme, 1961, 218-220.
4. DIGNAN P.S.J., MARTIN L.W. and ZENNI E J.: Pierre Robin anomaly with an accessory metacarpal of the index fingers (the Catel- Manzke syndrome). Clin Genet., 1986, 29, 168-173.
5. DUDIN A., ABDELSHAFI M. and RAMBAUD-COUSSON A.: Choledochal cyst associated with rare hand malformation. Am. J. Med. Genet., 1995, 56, 161-163.
6. FARNSWORTH P.B. and PACIK P.T.: Glossoptotic hypoxia and micrognathia - the Pierre Robin syndrome reviewed. Clin. Pediat., 1971, 10, 600-606.
7. GEWITZ M., DINWIDDIE R., YUILLE T., HILL E. and CARTER C.O.: Cleft palate and accessory metacarpal of index finger syndrome: possible familial occurrence. J. Med. Genet., 1978, 15, 162-164.
8. GORLIN R.J., CERVENKA J. and PRUZANSKY S.: Facial clefting and its syndromes. BDOAS, 1971, VII(7), 3-49.
9. GORLIN R.J., CERVENKA J., MOLLER K., HORROBIN M. and WITKOP C.J.: A selected miscellany. BDOAS, 1975, XI(2), 39- 50
10. . 10.HOLTHUSEN W.: The Pierre Robin unusual associated developmental defects. Annal. Radiol., 1972, 75, 253-262.
11. KLUG M.S., KETCHUM L.D. and LIPSEY J.H.: Symmetric hyperphalangism of the index finger in the palatodigital syndrome: a case report. J. Hand. Surg., 1983, 8, 599-603.
12. LIPSON A., BEULHER B., HARTLEY J., WALSH D., YU J., O'HALLORAM M. and WEBSTER W.: Maternal hyperphenylalaninemia fetal effects. J. Pediatr., 1984, 104, 216- 220.
13. MANZKE H.: Symmetrische Hyperphalangie des zweiten Fingers durch ein akzessorisches Metacarpale. Roefo., 1966, 105, 425-427.
14. PETIT P., MOERMAN P., LEGIUS E. and FRYNS J.P.: Catel-Manzke palatodigital syndrome in a second trimester female foetus with nuchal oedema, costovertebral anomalies and radial ray defect. Genet. Couns., 1994, 5, 381-385.
15. SILENGO M.C., FRANCESCHINI P., CERUTTI A. and FABRIS C.: Pierre Robin syndrome with hyperphalangism-clinodactylysm of the index finger: a possible new palato-digital syndrome. Pediat. Radiol., 1977, 6, 178-180.
16. SKINNER S.A., FLANNERY D.B. and STEVENSON R.E.: Catel-Manzke syndrome. Proc. Gr. Genet. Center., 1989, 8, 60-63.
17. STEVENSON R.E., TAYLOR H.A., BURTON O.M. and HEARN H.B.: A digitopalatal syndrome with associated anomalies of the heart, face, and skeleton. J. Med. Genet., 1980, 17, 238-242.
18. SUNDARAM V., TAYSI K., HARTMANN A.F., SHACKELFORD G.D. and KEATING J.P.: Hyperphalangy and clinodactyly of the index finger with Pierre Robin anomaly: Catel-Manzke syndrome. A case report and review of the literature. Clin. Genet., 1982, 21, 407-410.
19. THOMPSON E.M., WINTER R.M. and WILLIAMS M.J.H.: A male infant with the Catel-Manzke syndrome and dislocatable knees. J. Med. Genet., 1986, 25, 271-274.
20. WILSON G.N., KING T.E. and BROOKSHIRE G.S.: Index finger hyperphalangy and multiple anomalies : Catel-Manzke syndrome? Am. J. Med. Genet., 1993, 46, 176-179.