Cranioectodermal dysplasia (Sensenbrenner's syndrome).

Journal of medical genetics ·Vol. 26 ·No. 6 ·1989-06-00 ·Pages 393-6

Young ID

Abstract

暂无摘要

MeSH Terms

Abnormalities, Multiple Diseases in Twins Female Humans Infant Male Skin Abnormalities Skull/abnormalities Syndrome

Authors & Affiliations

1 authors, click to expand affiliations / ORCID

Young I D

Department of Child Health, Leicester Royal Infirmary.

References (9)

9 references, click to expand

New syndrome of skeletal, dental and hair anomalies.
Birth Defects Orig Artic Ser. 1975;11(2):372-9 PMID: 1227553
Craniosynostosis. I. Sagittal synostosis: its genetics and associated clinical findings in 214 patients who lacked involvement of the coronal suture(s).
Teratology. 1976 Oct;14(2):185-93 PMID: 982314
A heritable syndrome of craniosynostosis, short thin hair, dental abnormalities, and short limbs: cranioectodermal dysplasia.
J Pediatr. 1977 Jan;90(1):55-61 PMID: 830894
Cranioectodermal dysplasia.
Am J Dis Child. 1979 Dec;133(12):1275-6 PMID: 517478
Craniosynostosis and syndromes with craniosynostosis: incidence, genetics, penetrance, variability, and new syndrome updating.
Birth Defects Orig Artic Ser. 1979;15(5B):13-63 PMID: 393319
Tricho-dento-osseous syndrome: heterogeneity or clinical variability.
Am J Med Genet. 1983 Oct;16(2):225-36 PMID: 6650567
Growth retardation, alopecia, pseudo-anodontia, and optic atrophy--the GAPO syndrome: report of a patient and review of the literature.
Am J Med Genet. 1984 Oct;19(2):209-16 PMID: 6507471
DWARFISM IN THE AMISH I. THE ELLIS-VAN CREVELD SYNDROME.
Bull Johns Hopkins Hosp. 1964 Oct;115:306-36 PMID: 14217223
DWARFISM IN THE AMISH. II. CARTILAGE-HAIR HYPOPLASIA.
Bull Johns Hopkins Hosp. 1965 May;116:285-326 PMID: 14284412

Article Info

Journal

Journal of medical genetics

Abbr.

J Med Genet

ISSN

0022-2593

DOI

Published

1989-06-00

Pages

393-6

Language

English

Region

England

NLM ID

2985087R

PMCID

PMC1015626

Subset

External Links

Analysis Services