-transparent.png){kind=logo}
Jarcho-Levin syndrome is a variety of autosomal recessive spondylocostal dysostosis characterized by severe deformity of the thoracic cage, leading to respiratory failure and early death. There are often associated dysmorphic features. The disease is more frequent in Puerto Ricans and rare in Europe. A Sicilian family with four affected individuals in two interrelated sibships is reported.
Related Publications
M G Romeo, and
G Distefano, and
D Di Bella, and
A Mangiagli, and
L Caltabiano, and
S Roccaro, and
F Mollica
January 2001,
Ryoikibetsu shokogun shirizu,
M G Romeo, and
G Distefano, and
D Di Bella, and
A Mangiagli, and
L Caltabiano, and
S Roccaro, and
F Mollica
June 1994,
Indian pediatrics,
M G Romeo, and
G Distefano, and
D Di Bella, and
A Mangiagli, and
L Caltabiano, and
S Roccaro, and
F Mollica
September 1994,
Indian pediatrics,
M G Romeo, and
G Distefano, and
D Di Bella, and
A Mangiagli, and
L Caltabiano, and
S Roccaro, and
F Mollica
March 2006,
Indian journal of pediatrics,
M G Romeo, and
G Distefano, and
D Di Bella, and
A Mangiagli, and
L Caltabiano, and
S Roccaro, and
F Mollica
January 2000,
Ryoikibetsu shokogun shirizu,
M G Romeo, and
G Distefano, and
D Di Bella, and
A Mangiagli, and
L Caltabiano, and
S Roccaro, and
F Mollica
May 2002,
Pediatric neurosurgery,
M G Romeo, and
G Distefano, and
D Di Bella, and
A Mangiagli, and
L Caltabiano, and
S Roccaro, and
F Mollica
December 2003,
Current opinion in pediatrics,
M G Romeo, and
G Distefano, and
D Di Bella, and
A Mangiagli, and
L Caltabiano, and
S Roccaro, and
F Mollica
January 1993,
La Chirurgia degli organi di movimento,
M G Romeo, and
G Distefano, and
D Di Bella, and
A Mangiagli, and
L Caltabiano, and
S Roccaro, and
F Mollica
June 2018,
Indian journal of pediatrics,
M G Romeo, and
G Distefano, and
D Di Bella, and
A Mangiagli, and
L Caltabiano, and
S Roccaro, and
F Mollica
March 2004,
Puerto Rico health sciences journal,
