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Items: 2

1.

Spondylometaphyseal dysplasia, pagnamenta type

Spondylometaphyseal dysplasia Pagnamenta type (SMDP) is characterized by short stature and mild platyspondyly with no disproportion between the limbs. Mild metaphyseal changes are present (Pagnamenta et al., 2022). [from OMIM]

MedGen UID:
1794240
Concept ID:
C5562030
Disease or Syndrome
2.

Acromesomelic dysplasia 4

Acromesomelic dysplasia-4 (AMD4) is characterized by disproportionate short stature due to mesomelic shortening of the limbs. Radiographic hallmarks include mild to moderate platyspondyly, moderate brachydactyly, iliac flaring, and metaphyseal alterations of the long bones that progressively increase with age (Diaz-Gonzalez et al., 2022). For a discussion of genetic heterogeneity of acromesomelic dysplasia, see AMD1 (602875). [from OMIM]

MedGen UID:
1794238
Concept ID:
C5562028
Disease or Syndrome

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