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2.
Int J Oral Maxillofac Surg ; 16(2): 227-31, 1987 Apr.
Article in English | MEDLINE | ID: mdl-3110325

ABSTRACT

Thalassemia is an inherited genetic disorder of hemoglobin synthesis characterized by a reduction of either alpha or beta chains of globin. Typical features of patients with thalassemia are skeletal modifications, particularly in the skull and in the malar bone. This report describes a patient who was originally found to have an oro-facial deformity and subsequently demonstrated clinical and laboratory findings consistent with those recorded for thalassemia intermedia.


Subject(s)
Facial Asymmetry/etiology , Thalassemia/diagnosis , Child , Facial Bones/pathology , Female , Humans , Maxilla/pathology , Thalassemia/complications
3.
J Calif Dent Assoc (1961) ; 4(6): 65-6, 1976 Jun.
Article in English | MEDLINE | ID: mdl-1074863
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