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Facial Dysmorphic Features in a Patient With Nonketotic Hypoglycemia and a Pathogenic Variant in the AKT2 Gene
被引:3
作者:

Molina, Maria Fernanda Ochoa
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Pontificia Univ Catolica Chile, Sch Med, Div Pediat, Endocrinol Unit, Santiago, Chile
Pontificia Univ Catolica Chile, Sch Med, Div Pediat, Diagonal Paraguay 362, Santiago 8330077, Chile Pontificia Univ Catolica Chile, Sch Med, Div Pediat, Endocrinol Unit, Santiago, Chile

Poggi, Helena
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Pontificia Univ Catolica Chile, Sch Med, Div Pediat, Endocrinol Unit, Santiago, Chile Pontificia Univ Catolica Chile, Sch Med, Div Pediat, Endocrinol Unit, Santiago, Chile

De Toro, Valeria
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Pontificia Univ Catolica Chile, Sch Med, Dept Pediat Gastroenterol & Nutr, Santiago, Chile Pontificia Univ Catolica Chile, Sch Med, Div Pediat, Endocrinol Unit, Santiago, Chile

Mendoza, Carolina
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Pontificia Univ Catolica Chile, Sch Med, Div Pediat, Endocrinol Unit, Santiago, Chile Pontificia Univ Catolica Chile, Sch Med, Div Pediat, Endocrinol Unit, Santiago, Chile

Hussain, Khalid
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Sidra Med, Dept Pediat, Div Endocrinol, Doha, Qatar Pontificia Univ Catolica Chile, Sch Med, Div Pediat, Endocrinol Unit, Santiago, Chile
机构:
[1] Pontificia Univ Catolica Chile, Sch Med, Div Pediat, Endocrinol Unit, Santiago, Chile
[2] Pontificia Univ Catolica Chile, Sch Med, Dept Pediat Gastroenterol & Nutr, Santiago, Chile
[3] Sidra Med, Dept Pediat, Div Endocrinol, Doha, Qatar
[4] Pontificia Univ Catolica Chile, Sch Med, Div Pediat, Diagonal Paraguay 362, Santiago 8330077, Chile
关键词:
hyperinsulinism;
hypoglycemia;
overgrowth;
HYPOKETOTIC HYPOGLYCEMIA;
MUTATION;
D O I:
10.1016/j.aace.2021.11.006
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Background/Objective: AKT2 is a serine/threonine kinase that plays a key role in regulating insulin signaling. The phenotype related to the gain-of-function alteration in the AKT2 gene (c.49G>A, p.Glu17Lys) has been described in 5 patients with clinical findings that mimic hyperinsulinemic hypoglycemia but with undetectable levels of insulin and C-peptide. One of the reports highlights the facial dysmorphic features. We report the case of a new patient with the same activating AKT2 alteration leading to autonomous activation of the insulin signaling pathway and dysmorphic features. Moreover, to our knowledge, this is the first report using waxy maize heat-modified starch (WMHMS) in this condition. Case Report: A previously healthy child was evaluated at 6 months of age for episodes of hypoglycemia. The laboratory test results for the critical samples showed hypoketotic hypoglycemia (glucose level, 2.16 mmol/L [38 mg/dL]) with undetectable levels of insulin (<0.2 mU/L) and C-peptide (<0.033 nmol/L [reference range, 0.37-1.47 nmol/L]). Physical examination revealed hypertelorism, prominent proptosis of the eyes, a flat nasal bridge, delayed psychomotor development, and postnatal symmetrical overgrowth. The genetic study of AKT2 showed a pathogenic variant (c.49G>A, p.Glu17Lys). To achieve euglycemia, a diet of regular uncooked cornstarch (UCCS) carbohydrate was started. Subsequently, waxy maize heat-modified starch (WMHMS; Glycosade Vitaflo) was used to increase the fasting period to 4 hours. However, we did not find any advantages in comparison with UCCS. Discussion: The range of phenotypes of this gain-of-function alteration in AKT2 may be broad, including dysmorphic features, although the patients harbor the same pathogenic variant. Conclusion: Regarding the treatment, we observed a similar response with WMHMS compared with UCCS, with no adverse effects. (c) 2021 AACE. Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
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页码:109 / 112
页数:4
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Wellcome Trust Sanger Inst, Cambridge CB10 1SA, England Univ Cambridge, Metab Res Labs, Cambridge CB2 0QQ, England

Harris, J.
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Univ Cambridge, Metab Res Labs, Cambridge CB2 0QQ, England
Addenbrookes Hosp, Inst Metab Sci, Natl Inst Hlth Res, Cambridge Biomed Res Ctr, Cambridge CB2 0QQ, England Univ Cambridge, Metab Res Labs, Cambridge CB2 0QQ, England

Smillie, B. J. L.
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Univ Cambridge, Metab Res Labs, Cambridge CB2 0QQ, England
Addenbrookes Hosp, Inst Metab Sci, Natl Inst Hlth Res, Cambridge Biomed Res Ctr, Cambridge CB2 0QQ, England Univ Cambridge, Metab Res Labs, Cambridge CB2 0QQ, England

Savage, D. B.
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Univ Cambridge, Metab Res Labs, Cambridge CB2 0QQ, England
Addenbrookes Hosp, Inst Metab Sci, Natl Inst Hlth Res, Cambridge Biomed Res Ctr, Cambridge CB2 0QQ, England Univ Cambridge, Metab Res Labs, Cambridge CB2 0QQ, England

Ramaswami, U.
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Addenbrookes Hosp, Dept Paediat Endocrinol Diabet & Metab, Cambridge CB2 2QQ, England Univ Cambridge, Metab Res Labs, Cambridge CB2 0QQ, England

De Lonlay, P.
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Univ Paris 05, Hop Necker Enfants Malad, Dept Pediat, F-75743 Paris 15, France Univ Cambridge, Metab Res Labs, Cambridge CB2 0QQ, England

O'Rahilly, S.
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Univ Cambridge, Metab Res Labs, Cambridge CB2 0QQ, England
Addenbrookes Hosp, Inst Metab Sci, Natl Inst Hlth Res, Cambridge Biomed Res Ctr, Cambridge CB2 0QQ, England Univ Cambridge, Metab Res Labs, Cambridge CB2 0QQ, England

Barroso, I.
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Univ Cambridge, Metab Res Labs, Cambridge CB2 0QQ, England
Addenbrookes Hosp, Inst Metab Sci, Natl Inst Hlth Res, Cambridge Biomed Res Ctr, Cambridge CB2 0QQ, England
Wellcome Trust Sanger Inst, Cambridge CB10 1SA, England Univ Cambridge, Metab Res Labs, Cambridge CB2 0QQ, England

Semple, R. K.
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Univ Cambridge, Metab Res Labs, Cambridge CB2 0QQ, England
Addenbrookes Hosp, Inst Metab Sci, Natl Inst Hlth Res, Cambridge Biomed Res Ctr, Cambridge CB2 0QQ, England Univ Cambridge, Metab Res Labs, Cambridge CB2 0QQ, England