Experience of low-dose dexamethasone use in the respiratory management of ichthyosis prematurity syndrome

2021 ◽  
Vol 14 (8) ◽  
pp. e243348
Author(s):  
Davina Henderson ◽  
Claire A Murphy ◽  
Mary O'Dea ◽  
Michael A Boyle

Ichthyosis prematurity syndrome (IPS) is a rare disorder of autosomal recessive inheritance. The cardinal features include prematurity, vernix like hyperkeratosis, eosinophilia and neonatal asphyxiation. This case report discusses the presentation and management of IPS. We aim to characterise the common features, the spectrum of disease within a single family and discuss a potential role for low-dose dexamethasone in the management of ventilator-dependent patients with IPS.

2017 ◽  
Author(s):  
Caroline Lekszas ◽  
Barbara Vona ◽  
Indrajit Nanda ◽  
Reza Maroofian ◽  
Thomas Haaf

1992 ◽  
Vol 17 ◽  
pp. 222
Author(s):  
S. Mora ◽  
G. Weber ◽  
R.A. Adami ◽  
D. Pasolini ◽  
M.P. Guarneri ◽  
...  

2014 ◽  
Vol 2014 ◽  
pp. 1-2 ◽  
Author(s):  
Estela Morales-Peralta ◽  
Vivian Andrés ◽  
Dainé Campillo Betancourt

The scalp-ear-nipple (SEN) syndrome is an infrequent congenital disease. Its main features are scalp defects, malformed ears, and absence of nipples. Most of the reported cases are autosomal dominant. We report on a patient suffering SEN syndrome with possible autosomal recessive inheritance. It is concluded that SEN syndrome should be recognized as an entity with genetic heterogeneity once there is evidence of different genetic manner of inheritance described in this disease.


2014 ◽  
Vol 14 (1) ◽  
Author(s):  
Rui Yoshida ◽  
Toshihiko Kato ◽  
Masahiko Kawase ◽  
Mariko Honda ◽  
Tsuyoshi Mitsuishi

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