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April 27, 2026Düzce Tıp Fakültesi Dergisi0 citationsOpen Access

Bilateral Sensorineural Deafness and Congenital Malformation of the Middle, Internal Ear and Auditory Nerves in a Child with Pierpont Syndrome: A Case Report

LTLiya Vladimirovna ToropchinaЗИЗеликович Елена ИсааковнаМНМартынович Наталья Николаевна

Key Points

  • To present a clinical case of a child with bilateral deafness and symptoms of Pierpont syndrome.
  • Case report of a 3-year-old boy diagnosed with Pierpont syndrome.
  • Conducted genetic counseling and imaging studies including computed tomography and MRI of auditory nerves.
  • Reviewed literature related to auditory findings in Pierpont syndrome.
  • The child exhibited bilateral total deafness, motor delays, and hypotonia.
  • Imaging revealed malformations of the middle and internal ear, along with auditory nerve abnormalities.
  • Emphasized the significance of genetic evaluation for accurate diagnosis in similar cases.

Abstract

The case report aimed to present a clinical case of a 3-year-old boy, who presented first with motor delay at 3 months, later with bilateral total deafness and hypotonia, and was diagnosed as Pierpont syndrome with an autosomal dominant inheritance after a genetic counseling. Pierpont syndrome is a rare sporadic genetic disorder characterized by a general developmental delay, unusual facial features, abnormal fat distribution in the distal limbs, and hearing loss. The literature review is made, the hearing condition of the case is described, computed tomography findings of the temporal bones and 3 Tesla magnetic resonance imaging of the auditory nerves are presented. This case report, describing the audiologic picture in Pierpont syndrome, emphasizes the importance of referring patients with hearing loss to a geneticist and thoroughly examining. In addition to clinical findings, genetic evaluation is of great importance in the diagnosis of this rare syndrome.

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Cite This Study

Toropchina et al. (2026) studied this question.

synapsesocial.com/papers/69eefdb5fede9185760d470chttps://doi.org/10.18678/dtfd.1808235
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