Authors

Said Al Hanshi

Publications 4

Research article Open access

Diaphragmatic Paralysis Following Chest Tube Insertion in an Infant: Case report and literature review

Mohammed Al Ghafri, Said Al Hanshi, Ahmad E. Fouad et al. · Sultan Qaboos University Medical Journal · 2025 · 10.18295/squmj.10.2024.060

Diaphragmatic paralysis (DP) can occur due to central nervous system pathology or peripheral nerve injury. Direct injury to the phrenic nerve after intercostal chest drain (ICD) insertion for treatment of pneumothorax is an infrequent complication. We present a 4-month-old infant, ex-preterm 27 weeks, who was admitted …

Research article Open access

Two Cases of Pneumatoceles in Mechanically Ventilated Infants

Mohammed Al Ghafri, Said Al Hanshi, Suad Al-Ismaily · Oman Medical Journal · 2015 · 10.5001/omj.2015.59

Pulmonary pneumatocele is a thin-walled, gas-filled space within the lung that usually occurs in association with bacterial pneumonia and is usually transient. The majority of pneumatoceles resolve spontaneously without active intervention, but in some cases they might lead to pneumothorax with subsequent hemodynamic i …

Research article Open access

Severe Pertussis Pneumonia managed with Exchange Transfusion

Said Al Hanshi, Mohammed Al Ghafri, Suad Al Ismaili · Oman Medical Journal · 2014 · 10.5001/omj.2014.65

We describe in this case report one month old baby admitted to our Pediatric Intensive Care Unit (PICU) with severe pertussis pneumonia. The baby was deteriorating despite being on supportive management including High Frequency Oscillator ventilation (HFOV). However, she showed dramatic improvement after exchange blood …

Research article Open access

Late Onset Central Hypoventilation Syndrome due to a Heterozygous Polyalanine Repeat Expansion Mutation in the PHOX2B Gene

Ismail Al Rashdi, Mohammed Al Ghafri, Said Al Hanshi et al. · Oman Medical Journal · 2011 · 10.5001/omj.2011.87

This report describes a 6 year old girl with late onset central hypoventilation syndrome due to a heterozygous polyalanine repeat expansion mutation in the PHOX2B gene. This report aims to increase the awareness of this condition among physicians to allow earlier clinical and genetic diagnosis and management of cases o …

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