Azzarelli V, Roessmann U. Pathogenesis of central nervous system infiltration in acute leukemia. Arch Pathol Lab Med 1977; 101:203-5

Barness LA. Nutrition and nutritional disorders. In: Behrman RE, Vaughan VC (eds.) Nelson textbook of pediatrics. W.B. Saunders Company, Philadelphia, 1987 (13th ed.), pp. 11354

Boyadjiev SA, Justice CM, Eyaid W, McKusick VA, Lachman RS, Chowdry AB, Jabak M, Zwaan J, Wilson AF, Jabs EW. A novel dysmorphic syndrome with open calvarial sutures and sutural cataracts maps to chromosome 14q13-q21. Hum Genet 2003; 113: 1-9

Brandt I, Hodes DT, Reimnitz P. Anterior fontanelle as a window to the brain. Normal values and timing of closure. Klin Padiatr 1986; 198: 330-6

Capitanio MA, Kirkpatrick JA. Widening of the cranial sutures. A roentgen observation during periods of accelerated growth in patients treated for deprivation dwarfism. Radiology 1969; 92: 53-9

Cargile CB, McIntosh I, Clough MV, Rutberg J, Yaghmai R, Goodman BK, Chen XN, Korenberg JR, Thomas GH, Ger-aghty MT. Delayed membranous ossification of the cranium associated with familial translocation (2;3)(p15;q12). Am J Med Genet 2000; 92: 328-35

Chirathivat S, Post MJ. CT demonstration of dural metastases in neuroblastoma. J Comput Assist Tomogr 1980; 4: 316-9

Coussement A, Fauré C, Coussement-Beylard N. Repères et mesures en imagerie médicale. Expansion Scientifique Française, Paris, 1990 (4th ed), p. 60 Duc G, Largo RH. Anterior fontanel: size and closure in term and preterm infants. Pediatrics 1986; 78:904-8 Furuya Y, Edwards MS, Alpers CE, Tress BM, Ousterhout DK, Norman D. Computerized tomography of cranial sutures. 1. Comparison of suture anatomy in children and adults. J Neurosurg 1984; 61: 53-8 Gonzalez-del Angel A, Carnevale A, Takenaga R. Delayed membranous cranial ossification in a mother and child. Am J Med Genet 1992; 44: 786-9 Gorlin RJ, Whitley CB. Lenz-Majewski syndrome. Radiology

1983;149: 129-31 Holmes RD, Kuhns LR, Oliver WJ. Widened sutures in childhood meningitis: unrecognized sign of an acute illness.AJR Am J Roentgenol 1977; 128: 977-9 Jabs EW. Toward understanding the pathogenesis of cran-iosynostosis through clinical and molecular correlates. Clin Genet 1998; 53:79-86 Jarvis JL, Keats TE. Cleidocranial dysostosis. A review of 40 new cases. Am J Roentgenol Radium Ther Nucl Med 1974; 121:5-16

Jensen BL, Kreiborg S. Development of the skull in infants with cleidocranial dysplasia. J Craniofac Genet Dev Biol 1993; 13:89-97

Lyall H, Ogston SA, Paterson CR. Anterior fontanelle size in

Scottish infants. Scott Med J 1991; 36: 20-2 Manzanares MC, Goret-Nicaise M, Dhem A. Metopic sutural closure in the human skull. J Anat 1988; 161:203-15 Margulies SS, Thibault KL. Infant skull and suture properties: measurements and implications for mechanisms of pedi-atric brain injury. J Biomech Eng 2000; 122:364-71 Mundlos S, Otto F, Mundlos C, Mulliken JB, Aylsworth AS, Albright S, Lindhout D, Cole WG, Henn W, Knoll JH, Owen MJ, Mertelsmann R, Zabel BU, Olsen BR. Mutations involving the transcription factor CBFA1 cause cleidocranial dyspla-sia. Cell 1997; 89: 773-9 Park W, Paust H, Kaufmann HJ, Offermann G. Osteomalacia of the mother - rickets of the newborn. Eur J Pediatr 1987; 146: 292-3

Silverman FN, Byrd SE, Fitz CR. The skull, spine, and central nervous system. In: Silverman FN, Kuhn JP: Caffey's pediatric X-rays diagnosis. An integrated imaging approach. C.V. Mosby Company, St. Louis, 1993 (9th ed.), pp. 4-16 Stankiewicz P, Thiele H, Baldermann C, Kruger A, Giannakud-is I, Dorr S, Werner N, Kunz J, Rappold GA, Hansmann I. Phenotypic findings due to trisomy 7p15.3-pter including the TWIST locus. Am J Med Genet 2001; 103: 56-62 Swischuk LE. The normal newborn skull. Semin Roentgenol 1974; 9: 101-13

Tan KL.Wide sutures and large fontanels in the newborn.Am J

Dis Child 1976; 130: 386-90 Wilkie AO, Tang Z, Elanko N, Walsh S, Twigg SR, Hurst JA, Wall SA, Chrzanowska KH, Maxson RE Jr. Functional haploin-sufficiency of the human homeobox gene MSX2 causes defects in skull ossification. Nat Genet 2000; 24: 387-90 Wuyts W, Cleiren E, Homfray T, Rasore-Quartino A, Vanhoe-nacker F, van Hul W The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500). J Med Genet 2000; 37: 916-20

Was this article helpful?

0 0
Hearing Aids Inside Out

Hearing Aids Inside Out

Have you recently experienced hearing loss? Most probably you need hearing aids, but don't know much about them. To learn everything you need to know about hearing aids, read the eBook, Hearing Aids Inside Out. The book comprises 113 pages of excellent content utterly free of technical jargon, written in simple language, and in a flowing style that can easily be read and understood by all.

Get My Free Ebook

Post a comment