Acta Med. 2022, 65: 41-43

https://doi.org/10.14712/18059694.2022.16

Transient Hyperphosphatasemia in a Child with Autism Spectrum Disorder

Štěpán Kutíleka, Eva Rondziková-Mlynarčíkováa, Kamila Pečenkováa, Richard Piknerb, Tomáš Šmídac, Eva Sládkovád, Tomáš Honzíke, Hana Kolářováe, Martin Magnere

aDepartment of Pediatrics, Klatovy Hospital, Klatovy, Czech Republic
bDepartment of Clinical Biochemistry, Klatovy Hospital, Klatovy, Czech Republic
cGeneral Pediatric Practitioner, Klatovy, Czech Republic
dDepartment of Pediatrics, Faculty Hospital in Pilsen and Faculty of Medicine in Pilsen, Charles University, Czech Republic
eDepartment of Pediatrics and Inherited Metabolic Disorders, Faculty Hospital in Prague and 1st Faculty of Medicine in Prague, Charles University, Czech Republic

Received February 28, 2022
Accepted April 28, 2022

Introduction: Autism spectrum disorder (ASD) is a neurodevelopmental disorder characterized by deficits in social communication and the presence of restricted interests and repetitive behaviors. Transient hyperphosphatasemia of infancy and early childhood (THI) is a benign laboratory disorder characterized by transiently extremely elevated activity of serum alkaline phosphatase (S-ALP). Case Report: We present a 21-month-old girl with a right leg limp, most probably due to reactive arthritis after febrile viral infection, and deterioration of psychomotor development with concomitant transient elevation of S-ALP (61.74 μkat/L; normal 2.36–7.68 μkat/L). Normal values of serum creatinine, aspartate-aminotransferase, alanin-aminotransferase, calcium, phosphate, together with normal wrist X-ray ruled out rickets or other bone or hepatic cause of high S-ALP. The S-ALP gradually decreased within 3 months, thus fulfilling the THI criteria. Screening for inborn errors of metabolism was negative and meticulous neurologic, psychologic and psychiatric assessment pointed to the diagnosis of autism spectrum disorder (ASD). There was no causal relationship between THI and ASD, as high S-ALP was an accidental and transient finding within the routine laboratory assessment. However, when THI occurs in a child with an onset of a new disorder, or with a pre-existing bone or liver disease, it might seriously concern the physician. Conclusion: Children with THI should be spared from extensive evaluations and unnecessary blood draws.

References

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