Short rib-polydactyly syndrome, Saldino-Noonan type

Orpha code: 93270OMIM code: 613091

Definition

A rare ciliopathy with major skeletal involvement characterized by short ribs with an extremely narrow thorax, very short limbs, absent or very small fibulae, severe metaphyseal dysplasia of tubular bones, post-axial polydactyly, and defective ossification in the calvaria, vertebrae, pelvis, and bones of the hands and feet. Congenital anomalies of multiple other organs have also been described, such as polycystic kidneys, transposition of the great vessels, and atretic lesions of the gastrointestinal and genitourinary tract. Hydrops fetalis may be observed at an early gestational age.

Disease data
Classification

Malformation syndrome

Synonyms
Short rib-polydactyly syndrome type 1
Zespół krótkie żebro-polidaktylia typu 1
ORPHA code
93270
OMIM code
613091
ICD10 code
Q77.2
ICD11 code
-

No additional description.

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