# Dolichocephaly, Arachnodactyly, Diplopia, and Distal Myopathy – Novel Phenotype of MICU1 Variant c.553C>T

**Authors:** Josef Finsterer, Awini Barwari

PMC · DOI: 10.7759/cureus.52672 · Cureus · 2024-01-21

## TL;DR

A 23-year-old woman with a rare MICU1 gene variant showed new physical and neurological symptoms, expanding the known effects of this genetic condition.

## Contribution

The paper reports a novel MICU1 variant phenotype including dolichocephaly, arachnodactyly, diplopia, and distal myopathy.

## Key findings

- The patient exhibited previously unreported features like dolichocephaly and arachnodactyly with a MICU1 variant.
- Symptoms included developmental delay, myopathy, and dysmorphia, managed through therapies and antidepressants.
- The case highlights greater phenotypic heterogeneity of MICU1-related disorders than previously recognized.

## Abstract

Pathogenic variants in mitochondrial calcium uptake 1 (MICU1) manifest phenotypically heterogeneously but most frequently in the brain and skeletal muscle. Dolichocephaly, arachnodactyly, diplopia, and distal myopathy have not been reported in carriers of a pathogenic MICU1 variant. The patient is a 23-year-old female with consanguineous parents (first cousins) who was a carrier of the homozygous MICU1 variant c.553C>T, phenotypically presenting with developmental delay, intellectual disability, ataxia, dysmorphia (dolichocephaly, arachnodactyly, clinodactyly, hypertelorism, wide nasal bridge), myopathy (ptosis, double vision, strabismus, distal limb weakness, diffuse wasting, hypotonia), hyperextensible joints and hyperkyphosis. Features not previously described were dolichocephaly, arachnodactyly, broad nasal bridge, double vision, and distal myopathy. She was treated with physical therapy, speech therapy, and occupational therapy and received escitalopram and mirtazapine for concomitant depression, anxiety disorder, and insomnia. The presented case shows that the phenotypic heterogeneity of pathogenic MICU1 variants is even greater than previously assumed. Treatment of MICU1-related phenotypes is symptomatic, but these patients benefit from physical therapy, behavioral therapy, speech therapy, and antidepressant treatment.

## Linked entities

- **Genes:** MICU1 (mitochondrial calcium uptake 1) [NCBI Gene 10367]
- **Chemicals:** escitalopram (PubChem CID 146570), mirtazapine (PubChem CID 4205)
- **Diseases:** depression (MONDO:0002050), anxiety disorder (MONDO:0005618), insomnia (MONDO:0013600), distal myopathy (MONDO:0018949)

## Full-text entities

- **Genes:** MICU1 (mitochondrial calcium uptake 1) [NCBI Gene 10367] {aka CALC, CBARA1, EFHA3, MPXPS, ara CALC}
- **Diseases:** developmental delay (MESH:D002658), diffuse wasting (MESH:D019282), ptosis (MESH:C564553), anxiety disorder (MESH:D001008), Diplopia (MESH:D004172), dysmorphia (MESH:C537340), myopathy (MESH:D009135), intellectual disability (MESH:D008607), clinodactyly (MESH:C537090), Arachnodactyly (MESH:D054119), strabismus (MESH:D013285), hypertelorism (MESH:D006972), Distal Myopathy (MESH:D049310), broad nasal bridge (MESH:D054084), depression (MESH:D003866), insomnia (MESH:D007319), hyperextensible joints (MESH:C536192), distal limb weakness (MESH:D018908), ataxia (MESH:D001259), hyperkyphosis (MESH:D007738), hypotonia (MESH:D009123)
- **Chemicals:** escitalopram (MESH:D000089983), mirtazapine (MESH:D000078785)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** c.553C>T

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC10878678/full.md

## References

16 references — full list in the complete paper: https://tomesphere.com/paper/PMC10878678/full.md

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Source: https://tomesphere.com/paper/PMC10878678