Raine syndrome

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Raine syndrome (also called osteosclerotic bone dysplasia) is a rare disease in newborns characterized by craniofacial anomalies including microcephaly, exophthalmos, midface hypoplasia, cleft palate, gum hypertrophy and generalized osteosclerosis on radiography. It is usually lethal within a few hours after birth.

References

• Kan A, Kozlowski K (1992). "New distinct lethal osteosclerotic bone dysplasia (Raine syndrome).". Am J Med Genet 43 (5): 860-4. PMID 1642277.
• Rejjal A (1998). "Raine syndrome.". Am J Med Genet 78 (4): 382-5. PMID 9714445.
• Rickert C, Rieder H, Rehder H, Hülskamp G, Hörnig-Franz I, Louwen F, Paulus W (2002). "Neuropathology of Raine syndrome.". Acta Neuropathol (Berl) 103 (3): 281-7. PMID 11907809.
• Al-Gazali L, Jehier K, Nazih B, Abtin F, Haas D, Sadagahatian R (2003). "Further delineation of Raine syndrome.". Clin Dysmorphol 12 (2): 89-93. PMID 12868469.

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Acknowledgement and Attribution Regarding Sources of Content

Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .