Familial Clustering of Unexplained Transient Respiratory Distress in 12 Newborns from Three Unrelated Families Suggests an Autosomal-Recessive Inheritance

Author:

Guala Andrea1,Carrera Paola2,Pastore Guido3,Somaschini Marco4,Ancora Gina5,Faldella Giacomo5,De Filippi Paolo6,Ferrero Federica7,Guarino Roberta1,Danesino Cesare6

Affiliation:

1. SOC Pediatria Osp., Castelli Verbania, Italy

2. Laboratorio di Biologia Molecolare Clinica, IRCCS Osp. S. Raffaele Milano, Italy

3. SOC Pediatria, Osp. S.Andrea, Vercelli, Italy

4. SOC Neonatologia e Patologia Neonatale, Osp. Bolognini, Seriate, Italy

5. Istituto di Neonatologia, Università di Bologna, Italy

6. Genetica Medica, Università di Pavia e IRCCS S. Matteo, Pavia, Italy

7. Clinica Pediatrica, Università del Piemonte Orientale, Novara, Italy

Abstract

We report on 12 near-term babies from three families in which an unexplained transient respiratory distress was observed. No known risk factor was present in any family and no sequelae were recorded at follow-up. The most common causes of respiratory distress at birth are Neonatal Respiratory Distress Syndrome (NRD) and Transient Tachypnea of the Newborn (TTN), and their cumulative incidence is estimated to be about 2%. Genetic factors have been identified in NRD (surfactant genes) or suggested for TTN (genes affecting lung liquid clearance). Survivors from NRD may develop clinically relevant sequelae, while TTN does not cause any problem later in life. Our cases do not immediately fit NRD or TTN, while familial recurrence suggests the existence of a previously unreported subgroup on patients with respiratory distress for which autosomal-recessive inheritance is likely.

Publisher

Hindawi Limited

Subject

General Environmental Science,General Biochemistry, Genetics and Molecular Biology,General Medicine

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