Respiratory Medicine Case Reports (Jan 2015)

Hereditary mucoepithelial dysplasia and severe respiratory distress

  • Mahmoud Halawa,
  • Mutasim N. Abu-Hasan,
  • Mai K. ElMallah

DOI
https://doi.org/10.1016/j.rmcr.2015.03.004
Journal volume & issue
Vol. 15, no. C
pp. 27 – 29

Abstract

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Hereditary mucoepithelial dysplasia (HMD) is a rare autosomal dominant disorder characterized by mucoepithelial disruption of the skin, hair and mucous membranes. It results from defective gap junction formation and leads to non-scarring alopecia, mucosal erythema, perineal erythematous intertrigo, involvement of the conjunctival mucosa, and pulmonary disease. We present a case of severe respiratory distress in an initially healthy full term infant born to a mother with HMD. This infant later developed signs and symptoms of HMD. A high index of suspicion for pulmonary infection with atypical organism is essential in infants with a family history of HMD who present with respiratory distress.

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