2026-07-05T17:56:55Zhttps://repisalud.isciii.es/rest/oai/requestoai:repisalud.isciii.es:20.500.12105/140432025-03-12T09:47:26Zcom_20.500.12105_5571com_20.500.12105_2404com_20.500.12105_2403col_20.500.12105_5712
Repisalud
author
Pronzato Cuello, Flavia
author
Lázaro Carreño, María Isabel
2022-04-18T11:36:33Z
2022-04-18T11:36:33Z
2008-10
Boletín del ECEMC: Rev Dismor Epidemiol 2008; V (nº 7): 10-13
0210–3893
Boletín del ECEMC: Revista de Dismorfología y Epidemiología
http://hdl.handle.net/20.500.12105/14043
Michelin baby is a rare syndrome characterized by generalized folds of redundant skin. These features can be present alone or be associated with noncutaneous anomalies. The diagnosis is mainly clinical and it probable reflects multiple underlying disorders. Since the first description by Ross in 1969, approximately 20 patients have been reported. This paper describes a case of an 18-month-old girl with increased skin folds associated to facial dysmorphism and development delay, including a small review of the literature to contribute to a better understanding of this syndrome.
spa
Síndrome de Múltiples pliegues benignos de la piel de los miembros (síndrome de bebé Michelín)
research article
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URL
https://repisalud.isciii.es/bitstreams/5861efa8-392a-491a-bbc9-0fccb5f46e9f/download
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3120300
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SíndromeMúltiplesPlieguesBenignos_2008.pdf
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https://repisalud.isciii.es/bitstreams/aaeb2e08-6a01-433a-b05a-7e3ca088db8b/download
File
MD5
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text/plain
SíndromeMúltiplesPlieguesBenignos_2008.pdf.txt