Skip to main content

. 1969 Sep;6(3):266–274. doi: 10.1136/jmg.6.3.266

Camptodactyly, cleft palate, and club foot. A syndrome showing the autosomal-dominant pattern of inheritance.

H Gordon, D Davies, M Berman

PMCID: PMC1468739 PMID: 5345097

266

Images in this article

Fig. 2.
on p.267

Fig. 3.
on p.268

Fig. 4.
on p.268

Fig. 5.
on p.269

Fig. 6.
on p.269

Fig. 7.
on p.270

Fig. 8.
on p.270

Fig. 9.
on p.271

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

BAIRD H. W., 3rd KINDRED SHOWING CONGENITAL ABSENCE OF THE DERMAL RIDGES (FINGERPRINTS) AND ASSOCIATED ANOMALIES. J Pediatr. 1964 May;64:621–631. doi: 10.1016/s0022-3476(64)80610-7. [DOI] [PubMed] [Google Scholar]
BARINKA L. NOTES ON CAMPYLODACTYLIA. II. Acta Chir Plast. 1964;6:154–161. [PubMed] [Google Scholar]
CURRARINO G., WALDMAN I. CAMPTODACTYLY. Am J Roentgenol Radium Ther Nucl Med. 1964 Dec;92:1312–1321. [PubMed] [Google Scholar]
Dodge J. A., Kernohan D. C. Oral-facial-digital syndrome. Arch Dis Child. 1967 Apr;42(222):214–219. doi: 10.1136/adc.42.222.214. [DOI] [PMC free article] [PubMed] [Google Scholar]
EDWARDS J. H., HARNDEN D. G., CAMERON A. H., CROSSE V. M., WOLFF O. H. A new trisomic syndrome. Lancet. 1960 Apr 9;1(7128):787–790. doi: 10.1016/s0140-6736(60)90675-9. [DOI] [PubMed] [Google Scholar]
EVERED D. F. The excretion of amino acids by the human; a quantitative study with ion-exchange chromatography. Biochem J. 1956 Mar;62(3):416–427. doi: 10.1042/bj0620416. [DOI] [PMC free article] [PubMed] [Google Scholar]
GILLESPIE F. D. A HEREDITARY SYNDROME: "DYSPLASIA OCULODENTODIGITALIS. Arch Ophthalmol. 1964 Feb;71:187–192. doi: 10.1001/archopht.1964.00970010203009. [DOI] [PubMed] [Google Scholar]
GORLIN R. J., MESKIN L. H., PETERSON W. C., Jr, GOLTZ R. W. FOCAL DERMAL HYPOPLASIA SYNDROME. Acta Derm Venereol. 1963;43:421–440. [PubMed] [Google Scholar]
Hecht F., Jarvinen J. M. Heritable dysmorphic syndrome with normal intelligence. J Pediatr. 1967 Jun;70(6):927–937. doi: 10.1016/s0022-3476(67)80265-8. [DOI] [PubMed] [Google Scholar]
LARSEN L. J., SCHOTTSTAEDT E. R., BOST F. C. Multiple congenital dislocations associated with characteristic facial abnormality. J Pediatr. 1950 Oct;37(4):574–581. doi: 10.1016/s0022-3476(50)80268-8. [DOI] [PubMed] [Google Scholar]
MOLDENHAUER E. ZUR KLINIK DES NIELSON-SYNDROMS. Dermatol Wochenschr. 1964 Dec 5;150:594–601. [PubMed] [Google Scholar]
Neel J. V., Rusk M. L. Polydactyly of the Second Metatarsal with Associated Defects of the Feet: A New, Simply Inherited Skeletal Deformity. Am J Hum Genet. 1963 Sep;15(3):288–291. [PMC free article] [PubMed] [Google Scholar]
Nevin N. C., Hurwitz L. J., Neill D. W. Familial camptodactyly with taurinuria. J Med Genet. 1966 Dec;3(4):265–268. doi: 10.1136/jmg.3.4.265. [DOI] [PMC free article] [PubMed] [Google Scholar]
PARISH J. G., HORN D. B., THOMPSON M. FAMILIAL STREBLODACTLY WITH AMINO-ACIDURIA. Br Med J. 1963 Nov 16;2(5367):1247–1250. doi: 10.1136/bmj.2.5367.1247. [DOI] [PMC free article] [PubMed] [Google Scholar]
PATAU K., SMITH D. W., THERMAN E., INHORN S. L., WAGNER H. P. Multiple congenital anomaly caused by an extra autosome. Lancet. 1960 Apr 9;1(7128):790–793. doi: 10.1016/s0140-6736(60)90676-0. [DOI] [PubMed] [Google Scholar]
SOUPART P. Urinary excretion of free amino acids in normal adult men and women. Clin Chim Acta. 1959 Mar;4(2):265–271. doi: 10.1016/0009-8981(59)90140-8. [DOI] [PubMed] [Google Scholar]
Taylor A. I. Patau's, Edwards' and Cri du Chat syndromes: a tabulated summary of current findings. Dev Med Child Neurol. 1967 Feb;9(1):78–86. doi: 10.1111/j.1469-8749.1967.tb02213.x. [DOI] [PubMed] [Google Scholar]
Taylor W. B., Lane D. K. Congenital fistulas of the lower lip. Associations with cleft lip-palate and anomalies of the extremities. Arch Dermatol. 1966 Oct;94(4):421–424. [PubMed] [Google Scholar]
WILSON R. Marfan's syndrome: description of a family. Am J Med. 1957 Sep;23(3):434–444. doi: 10.1016/0002-9343(57)90323-6. [DOI] [PubMed] [Google Scholar]
WYNNE-DAVIES R. FAMILY STUDIES AND THE CAUSE OF CONGENITAL CLUB FOOT. TALIPES EQUINOVARUS, TALIPES CALCANEO-VALGUS AND METATARSUS VARUS. J Bone Joint Surg Br. 1964 Aug;46:445–463. [PubMed] [Google Scholar]
Welch J. P., Temtamy S. A. Hereditary contractures of the fingers (camptodactyly). J Med Genet. 1966 Jun;3(2):104–113. doi: 10.1136/jmg.3.2.104. [DOI] [PMC free article] [PubMed] [Google Scholar]

ACTIONS

RESOURCES