Case Report
Mendelian Susceptibility to Mycobacterial Diseases (MSMD) in a 13-Year-Old Ethiopian Girl with Autosomal Dominant Interferon Gamma Receptor 1(IFN-γ R1) Defect: A Clinical Diagnostic and Treatment Challenge
Figure 7
(a) and (b) Skull X-ray of the 13 years old girl with MSMD from Ethiopia: multiple trans-diploic lesions with inner and outer calvarial bone destruction; findings were suggestive of delayed/arrested sphenoid sinus pneumatization.
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