Teaching point
This case illustrates very well what Ralph Waldo Emerson said: "People only see what they are prepared to see.†If you are not aware of the existence of an anomaly it is very easy to glance over it. Hopefully, none will ever miss a bone spur again !
The other point worth making is that especially when dealing with very rare syndromes relying on what one knows may not often be sufficient. The usual process to get help is typically looking in Medline, OMIM and (hey why not ? I know it is still beginning) The Fetus. Note that no reference is ideal. As you will see the important articles that allow this diagnosis are both in a journal called "Dysmorphology and Clinical Genetics†that is not indexed in Medline.
References
More info at Hypophosphatasia
Goldstein, D. J., Nichols, W. C., Mirkin, L. D.: Short-limbed osteochondrodysplasia with osteochondral spurs of knee and elbow joints (spur-limbed dwarfism). Dysmorph. Clin. Genet. 1: 12-16, 1987.
Shohat, M., Rimoin, D. L., Gruber, H. E., Lachman, R. S.: Perinatal lethal hypophosphatasia: clinical, radiologic and morphologic findings. Pediat. Radiol. 21: 421-427, 1991.
Spranger, J.: "Spur-limbed†dwarfism identified as hypophosphatasia. (Letter) Dysmorph. Clin. Genet. 2: 123, 1988.
Benzie R, Doran TA, Escoffery W, Gardner HA, Hoar DI, Hunter A, Malone R, Miskin M, Rudd NL Prenatal diagnosis of hypophosphatasia. Birth Defects Orig Artic Ser 1976,12(6):271-82
Terada S, Suzuki N, Ueno H, Uchide K, Kohama T: A congenital lethal form of hypophosphatasia: histologic and ultrastructural study. Acta Obstet Gynecol Scand 1996 May;75(5):502-5
Tongsong T, Sirichotiyakul S, Siriangkul S Prenatal diagnosis of congenital hypophosphatasia. J Clin Ultrasound 1995 Jan;23(1):52-5
Kleinman G, Uri M, Hull S, Keene C Perinatal ultrasound casebook. Antenatal findings in congenital hypophosphatasia. J Perinatol 1991 Sep;11(3):282-4
Wladimiroff JW, Niermeijer MF, Van der Harten JJ, Stewart PA, Versteegh FG, Blom W, Huijmans JG Early prenatal diagnosis of congenital hypophosphatasia: case report. Prenat Diagn 1985 Jan-Feb;5(1):47-52