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Smith-Lemli-Opitz syndrome presenting as acute adrenal crisis in a child: a case report

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dc.contributor.author Jayamanne, C.
dc.contributor.author Sandamal, S.
dc.contributor.author Jayasundara, K.
dc.contributor.author Saranavananthan, M.
dc.contributor.author Mettananda, S.
dc.date.accessioned 2019-01-02T06:02:09Z
dc.date.available 2019-01-02T06:02:09Z
dc.date.issued 2018
dc.identifier.citation Journal of Medical Case Reports.2018;12(1):217 en_US
dc.identifier.issn 1752-1947 (Electronic)
dc.identifier.issn 1752-1947 (Linking)
dc.identifier.uri http://repository.kln.ac.lk/handle/123456789/19236
dc.description Indexed In MEDLINE en_US
dc.description.abstract BACKGROUND: Smith-Lemli-Opitz syndrome is a rare autosomal recessive disorder of cholesterol biosynthesis which is characterized by multiple congenital malformations and global developmental delay. Here we report the case of a 3-year-old, previously undiagnosed, child with Smith-Lemli-Opitz syndrome presenting with acute adrenal crisis, which is an extremely rare and atypical presentation of this disease. CASE PRESENTATION: A 3-year-old Sri Lankan Sinhalese boy without evidence of infection presented with circulatory collapse. He had a normal perinatal period; however, his early infancy was complicated by poor feeding, episodes of loose stools, failure to thrive, and several episodes of unexplained drowsiness. His weight, height, and occipitofrontal circumference were well below the third percentile. He had soft dysmorphic features that included microcephaly, bitemporal narrowing, upward slanting eyes, epicanthal folds, partial ptosis, broad nasal bridge, low set posteriorly rotated ears, high arched palate, and short neck. Marked hyperpigmentation was noted in perioral, buccal, and palmar areas. His pulses were rapid and low in volume and his systolic blood pressure was low. Initial resuscitation was performed by administering multiple crystalloid fluid boluses. A septic screen was negative. His blood glucose and serum bicarbonate levels were low and serum electrolytes revealed hyponatremia with hyperkalemia. Serum spot cortisol level was low normal and 17-hydroxyprogesterone level was low. Diagnosis of Smith-Lemli-Opitz syndrome and associated adrenal crisis was made based on clinical and biochemical features. Intravenously administered hydrocortisone was commenced to which he showed a marked clinical response. CONCLUSIONS: This case describes a rare and atypical presentation of Smith-Lemli-Opitz syndrome and highlights the importance of making early and accurate syndromic diagnoses in children with dysmorphism to avoid sudden and life-threatening complications. en_US
dc.language.iso en_US en_US
dc.publisher BioMed Central en_US
dc.subject Smith-Lemli-Opitz Syndrome en_US
dc.subject Smith-Lemli-Opitz Syndrome-diagnosis en
dc.subject Adrenal Insufficiency
dc.subject Adrenal Insufficiency-diagnosis en
dc.subject Case Reports en
dc.subject Child en
dc.title Smith-Lemli-Opitz syndrome presenting as acute adrenal crisis in a child: a case report en_US
dc.type Case Report en_US


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