Abstract

Introduction: We aimed to summarize the clinical characteristics of Floating-Harbor syndrome (FHS) and the effect of recombinant human growth hormone (rhGH) to increase height.Methods: The clinical manifestations, gene sequencing results, treatment, and regression of one child with FHS were reported at the Department of Pediatrics, General Hospital of Tianjin Medical University, in July 2020. PubMed was searched using the keyword “Floating-Harbor Syndrome” up to March 2021 to obtain clinical information on children with FHS for review.Results: The child, who was a male aged 6 years and 9 months, presented to the clinic with main complaints of delayed language development since childhood and a short stature for 4 years. The child's short stature, peculiar facial features, delayed language development, and delayed bone development were considered alongside genetic testing and Sanger sequencing to verify the results. A heterozygous mutation (c.7401delC; p.Ile2468Phefs*7) was identified in exon 34 of the SRCAP gene, which was a frameshift mutation, and Sanger verification showed that neither parent had this mutation. The child was administered subcutaneous injection of rhGH (0.13 U/kg/day) and was followed up regularly. At the time of writing, the child had been treated for 6 months and was 7 years and 3 months old with a height of 106.3 cm (−3.69 SDS), which was a height increase of 6.3 cm. The patient did not complain of discomfort during treatment and presented normal laboratory tests results. Twenty-two children with FHS treated with rhGH were included in the literature review, and most of these patients demonstrated an increase in height SDS without adverse effects.Conclusion: Short stature, delayed skeletal maturation, impaired language expression, intellectual deficits, and peculiar facial features are the main clinical features of FHS. rhGH can be used as a treatment to increase height in patients with FHS, but its effectiveness and safety still need to be monitored in larger sample sizes over longer periods of time.

Highlights

  • We aimed to summarize the clinical characteristics of Floating-Harbor syndrome (FHS) and the effect of recombinant human growth hormone to increase height

  • We retrospectively analyzed the clinical data of a child with FHS who was treated with recombinant human growth hormone for a short stature

  • The results showed that a heterozygous mutation (c.7401delC; p.Ile2468Phefs∗7) was present in exon 34 of the SRCAP gene, which is a frameshift mutation that is not reported in the Human Gene Mutation Database

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Summary

Introduction

We aimed to summarize the clinical characteristics of Floating-Harbor syndrome (FHS) and the effect of recombinant human growth hormone (rhGH) to increase height. Floating-Harbor syndrome (FHS) is a rare autosomal dominant disorder. The main clinical features of FHS are short stature, peculiar facial features, and delayed speech development [1]. Typical characteristic facial features include a triangular face, deep-set eyes, long eyelashes, low-set ears, a wide nasal bridge, a short philtrum, a wide mouth, and thin lips. Most mutations are spontaneous mutations; there are occasional reports of autosomal dominant familial inheritance [2]. We retrospectively analyzed the clinical data of a child with FHS who was treated with recombinant human growth hormone (rhGH) for a short stature. We reviewed the relevant literature to provide a theoretical basis for clinical management of FHS

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