Mendelian Susceptibility to Mycobacterial Diseases (MSMD) in a 13-Year-Old Ethiopian Girl with Autosomal Dominant Interferon Gamma Receptor 1(IFN-<i>γ</i> R1) Defect: A Clinical Diagnostic and Treatment Challenge

<div>(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.</div>

Case Reports in Infectious Diseases

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Figure 7: Mendelian Susceptibility to Mycobacterial Diseases (MSMD) in a 13-Year-Old Ethiopian Girl with Autosomal Dominant Interferon Gamma Receptor 1(IFN-<i>γ</i> R1) Defect: A Clinical Diagnostic and Treatment Challenge 

Figure 7 | 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 