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

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...

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Autores principales: Jayamanne, Chamara, Sandamal, Sajith, Jayasundara, Kasun, Saranavabavananthan, Mayoorathy, Mettananda, Sachith
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6085650/
https://www.ncbi.nlm.nih.gov/pubmed/30092813
http://dx.doi.org/10.1186/s13256-018-1738-4
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author Jayamanne, Chamara
Sandamal, Sajith
Jayasundara, Kasun
Saranavabavananthan, Mayoorathy
Mettananda, Sachith
author_facet Jayamanne, Chamara
Sandamal, Sajith
Jayasundara, Kasun
Saranavabavananthan, Mayoorathy
Mettananda, Sachith
author_sort Jayamanne, Chamara
collection PubMed
description 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.
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spelling pubmed-60856502018-08-16 Smith–Lemli–Opitz syndrome presenting as acute adrenal crisis in a child: a case report Jayamanne, Chamara Sandamal, Sajith Jayasundara, Kasun Saranavabavananthan, Mayoorathy Mettananda, Sachith J Med Case Rep Case Report 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. BioMed Central 2018-08-10 /pmc/articles/PMC6085650/ /pubmed/30092813 http://dx.doi.org/10.1186/s13256-018-1738-4 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Jayamanne, Chamara
Sandamal, Sajith
Jayasundara, Kasun
Saranavabavananthan, Mayoorathy
Mettananda, Sachith
Smith–Lemli–Opitz syndrome presenting as acute adrenal crisis in a child: a case report
title Smith–Lemli–Opitz syndrome presenting as acute adrenal crisis in a child: a case report
title_full Smith–Lemli–Opitz syndrome presenting as acute adrenal crisis in a child: a case report
title_fullStr Smith–Lemli–Opitz syndrome presenting as acute adrenal crisis in a child: a case report
title_full_unstemmed Smith–Lemli–Opitz syndrome presenting as acute adrenal crisis in a child: a case report
title_short Smith–Lemli–Opitz syndrome presenting as acute adrenal crisis in a child: a case report
title_sort smith–lemli–opitz syndrome presenting as acute adrenal crisis in a child: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6085650/
https://www.ncbi.nlm.nih.gov/pubmed/30092813
http://dx.doi.org/10.1186/s13256-018-1738-4
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