The Nager syndrome - Concepedia

Concepedia

Abstract

The Nager syndrome was identified in a newborn infant and in a subsequent sib by prenatal ultrasonography. This report documents an autosomal recessive pattern of inheritance for this disorder.

References

	Year	Citations
Acrofacial dysostosis with severe facial clefting and limb reduction E. L. Kawira, David D. Weaver, H. A. Bender, American Journal of Medical Genetics	1984	36
Familial gingival fibromatosis associated with progressive deafness in five generations of a family. Guy C. Jones, R. Sid Wilroy, Verna A. McHaney PubMed	1977	35
Syndrome of acrofacial dysostosis, cleft lip/palate, and triphalangeal thumb in a brazilian family A. Richieri‐Costa, Thomaz Rafael Gollop, G M D D Colletto, American Journal of Medical Genetics Brazilian FamilyNonconsanguineous CoupleRadial RaysDevelopmental AnomalyThumb Hypoplasia	1983	28
Acrofacial dysostosis (Nager syndrome): Synopsis and report of a new case R. A. Pfeiffer, H. Stoess, John M. Opitz American Journal of Medical Genetics Developmental AnomalyThumb HypoplasiaUpper LimbNew CaseCongenital Disorders	1983	28
Nager acrofacial dysostosis Barbara K. Burton, Henry L. Nadler The Journal of Pediatrics RheumatologyNager Acrofacial DysostosisClinical FindingAutoimmune DiseasePathogenesis	1977	27
Apparent autosomal recessive inheritance of the Treacher Collins syndrome. Walker Fa PubMed Down SyndromeTreacher Collins SyndromeMendelian DisorderGenetic DisorderGenetics	1974	17
Acrofacial dysostosis with growth and mental retardation in three males, one with simultaneous Hermansky-Pudlak syndrome. Kelly Te, Cooke Rj, Kester Rw Munich Personal RePEc Archive (Ludwig Maximilian University of Munich)	1977	11

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