Acromesomelic dysplasia, Maroteaux type

Orpha code: 40OMIM code: 602875

Definition

A rare autosomal recessive acromesomelic dysplasia characterized by severe dwarfism (adult height <120 cm), both axial and appendicular involvement (shortening of the middle and distal segments of limbs and vertebral shortening), and with normal facial appearance and intelligence. It is a less severe form than acromesomelic dysplasia, Grebe type and acromesomelic dysplasia, Hunter-Thomson type .

Disease data
Classification

Malformation syndrome

ORPHA code
40
OMIM code
602875
ICD10 code
Q77.8
ICD11 code
LD24.9

No additional description.

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