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Should We Stop Calling Thanatophoric Dysplasia a Lethal Condition? A Case Report of a Long-Term Survivor
Author(s) -
Ricki Carroll,
Angela L. Duker,
Andrea J. Schelhaas,
Mary Ellen Little,
Elissa Miller,
Michael B. Bober
Publication year - 2020
Publication title -
palliative medicine reports
Language(s) - English
Resource type - Journals
ISSN - 2689-2820
DOI - 10.1089/pmr.2020.0016
Subject(s) - palliative care , medicine , dysplasia , quality of life (healthcare) , pediatrics , intensive care medicine , psychology , family medicine , nursing , pathology
Thanatophoric dysplasia (TD) is a rare skeletal dysplasia commonly thought to be lethal. In this case report, we discuss a nine-year-old male with TD and review his parents' decision making shortly after their son was born, the technology needed to sustain him, and his parents' perception of his quality of life. We also summarize the clinical course of published long-term survivors with TD. Pediatric Palliative Care teams, especially those conducting perinatal palliative care consultations, are often asked to support families in the face of prognostic uncertainty. Our case report and review of the literature adds to the uncertainty of prognosis in TD and suggests that pediatric palliative care providers should be wary of the label “lethal.”

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