Robinow syndrome
Robinow syndrome noun: a rare genetic disorder characterized by short-limbed dwarfism, abnormalities in the head, face, and external genitalia, and vertebral segmentation.
Noun
Robinow syndrome (uncountable)
- A rare genetic disorder characterized by short-limbed dwarfism, abnormalities in the head, face, and external genitalia, and vertebral segmentation.
Origin of Robinow syndrome
First described in 1969 by human geneticist Meinhard Robinow.
Questions about Robinow syndrome
- What does Robinow syndrome mean?
- Robinow syndrome means a rare genetic disorder characterized by short-limbed dwarfism, abnormalities in the head, face, and external genitalia, and vertebral segmentation.
- What part of speech is Robinow syndrome?
- Robinow syndrome is a noun.
Words near Robinow syndrome in the dictionary
Source and license
Adapted from Wiktionary: Robinow 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.
Last updated:
Cite this entry: “Robinow syndrome.” Word.ws, https://word.ws/robinow_syndrome. Based on Wiktionary, CC BY-SA 4.0.
