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An Unusual Cause of Respiratory Distress in Term Neonate.


ABSTRACT: We report a female infant who was born at 41+6 weeks of gestation to a consanguineous parent, and the initial newborn examination was within normal. At 12 hours of age, she developed tachypnea; with desaturation, she had continuous thick whitish oral secretion. Admitted to the neonatal intensive care unit (NICU) for further management, her initial blood investigation, including blood gas and chest X-ray, was normal. Due to the persistent unexplained respiratory distress with a normal chest X-ray, we obtained a further history from parents with three siblings with respiratory symptoms but no definitive diagnosis. The genetic testing of whole-exome sequences (WES) confirmed a homozygous variant c.804_806del, p.(Lys268del) in the RSPH9 gene that causes primary ciliary dyskinesia (PCD). Her three siblings were tested and found to have the same genetic mutation.

SUBMITTER: Alallah JS 

PROVIDER: S-EPMC9428618 | biostudies-literature | 2022 Aug

REPOSITORIES: biostudies-literature

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An Unusual Cause of Respiratory Distress in Term Neonate.

Alallah Jubara S JS   Makki Reham R   Saber Arwa A AA   Moustafa Ahmed A   Ghandourah Hasan H  

Cureus 20220801 8


We report a female infant who was born at 41+6 weeks of gestation to a consanguineous parent, and the initial newborn examination was within normal. At 12 hours of age, she developed tachypnea; with desaturation, she had continuous thick whitish oral secretion. Admitted to the neonatal intensive care unit (NICU) for further management, her initial blood investigation, including blood gas and chest X-ray, was normal. Due to the persistent unexplained respiratory distress with a normal chest X-ray  ...[more]

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