Browsing Medicine by Author "Kamalanathan, P."

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Familial glucocorticoid deficiency presenting with hyperpigmentation, gigantism, and motor development delay: a case report.

Uyangoda, K.; Kamalanathan, P.; Mettananda, S. (BioMed Central,London, 2019)

BACKGROUND: Familial glucocorticoid deficiency is a rare autosomal recessive disorder characterized by isolated glucocorticoid deficiency. Most patients are diagnosed following episodes of hypoglycemia or convulsion. We ...
Spondylocostal Dysplasia in a 7-year-old Sri Lankan girl causing restrictive lung disease: A case report and review of the literature

Kamalanathan, P.; Fernando, M.; Jayawardena, R.; Upasena, A.; Rajindrajith, S.; Mettananda, S. (Hindawi Pub. Corp., 2020)

ABSTRACT: Spondylocostal dysplasia (SCD) is a rare costovertebral malformation characterised by short-trunk short stature. It is a recessively inherited disorder, and commonly identified disease-causing mutations are in ...
Streptococcus bovis - unusual etiology of meningitis in a neonate with Down syndrome: a case report

Mettananda, S.; Kamalanathan, P.; Dhananja Namalie, K. (BioMed Central, 2018)

BACKGROUND: Common etiological agents of neonatal meningitis include group B Streptococcus, Escherichia coli, and Staphylococcus aureus. Here we report a rare pathogen - Streptococcus bovis - causing meningitis in a premature ...

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