Total: 3 |
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PMID (PMCID) | ||
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11041444 |
FEMALE | Infant, Newborn |
Recurrent familial neonatal deaths: hereditary surfactant protein B deficiency. | ||
Andersen C, Ramsay JA, Nogee LM, Shah J, Wert SE, Paes B, Nowaczyk MJ. Am J Perinatol. 2000;17(4):219-24. |
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Previous deaths were mistakenly attributed to hyaline membrane disease (HMD), congenital Mycoplasma hominis infection, and pulmonary hypertension, however, following the diagnosis in the proposita, SP-B deficiency was also confirmed in her deceased siblings by immunohistochemical staining of autopsy specimens. | ||
7731416 |
FEMALE | Infant, Newborn |
[Efficacy of magnesium in a case of neonatal pulmonary hypertension refractory to the usual therapies]. | ||
Colonna F, Giorgi R, Ciana G, Benettoni A. Minerva Pediatr. 1994;46(12):553-5. |
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We describe a premature baby with X pentasomy, having a severe pulmonary hypertension secondary to perinatal asphyxia and hyaline membrane disease which appeared to be refractory to conventional treatments (hyperventilation, tolazoline, prostacyclin). | ||
2461271 |
MALE | |
Enhancing child compliance with nebulized respiratory treatment. A case study. | ||
Reimers TM, Piazza CC, Fisher WW, Parrish JM, Page TJ. Clin Pediatr (Phila). 1988;27(12):605-8. |
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A 2.7-year-old developmentally delayed boy diagnosed as having chronic lung disease, severe hyaline membrane disease, and persistent pulmonary hypertension with interstitial emphysema was referred in hopes of modifying his refusal to wear a mask during nebulized administrations of Chromolyn. |