Fitzsimmons-Guilbert syndrome
Fitzsimmons-Guilbert syndrome noun: a rare genetic disorder characterized by slowly progressive spastic paraplegia, skeletal anomalies of the hands and feet with brachydactyly type E, cone-shaped epiphyses, abnormal metaphyseal–phalangeal pattern profile, sternal anomaly (pectus carinatum or excavatum), dysarthria, and mild intellectual deficit.
Noun
Fitzsimmons-Guilbert syndrome (uncountable)
- A rare genetic disorder characterized by slowly progressive spastic paraplegia, skeletal anomalies of the hands and feet with brachydactyly type E, cone-shaped epiphyses, abnormal metaphyseal–phalangeal pattern profile, sternal anomaly (pectus carinatum or excavatum), dysarthria, and mild intellectual deficit.
Questions about Fitzsimmons-Guilbert syndrome
- What does Fitzsimmons-Guilbert syndrome mean?
- Fitzsimmons-Guilbert syndrome means a rare genetic disorder characterized by slowly progressive spastic paraplegia, skeletal anomalies of the hands and feet with brachydactyly type E, cone-shaped epiphyses, abnormal metaphyseal–phalangeal pattern profile, sternal anomaly (pectus carinatum or excavatum), dysarthria, and mild intellectual deficit.
- What part of speech is Fitzsimmons-Guilbert syndrome?
- Fitzsimmons-Guilbert syndrome is a noun.
Words near Fitzsimmons-Guilbert syndrome in the dictionary
Source and license
Adapted from Wiktionary: Fitzsimmons-Guilbert syndrome (page history and authors). Text available under the Creative Commons Attribution-ShareAlike 4.0 license. Word.ws reformatted the entry and added links. Wiktionary data of 2026-09-02.
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Cite this entry: “Fitzsimmons-Guilbert syndrome.” Word.ws, https://word.ws/fitzsimmons-guilbert_syndrome. Based on Wiktionary, CC BY-SA 4.0.
