Shwachman-Diamond syndrome (SDS) is an autosomal recessive bone marrow failure syndrome typically characterized by neutropenia and pancreatic dysfunction, although phenotypic presentations vary, and the endocrine phenotype is not well-described. We report a unique case of a patient with SDS who initially presented with hypoglycemia and micropenis in the newborn period and was diagnosed with congenital hypopituitarism. We are not aware of any other cases of SDS documented with this combination of complex endocrinopathies.
a preponderance of high-risk behaviors (elevated number of sexual partners and the absence of barrier protection during intercourse). This study highlights the critical need for targeted intervention programs aimed at reducing sexual risk behavior, as well as, illicit drug use with this high-risk population. Sources of Support: No outside support.
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