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Items: 4

1.

Acheiropodia

Acheiropody is characterized by bilateral congenital amputations of the upper and lower extremities and aplasia of the hands and feet. Specific patterns of malformations consist of a complete amputation of the distal epiphysis of the humerus, amputation of the distal part of the tibial diaphysis, and aplasia of the radius, ulna, fibula, and of the carpal, metacarpal, tarsal, metatarsal, and phalangeal bones (summary by Ianakiev et al., 2001). [from OMIM]

MedGen UID:
120547
Concept ID:
C0265559
Congenital Abnormality
2.

Split-hand/foot malformation with long bone deficiency 1

MedGen UID:
349310
Concept ID:
C1861553
Disease or Syndrome
3.

Acrofacial dysostosis Rodriguez type

A multiple malformation syndrome in which mandibulofacial dysostosis and severe limb reduction defects are associated with complex malformations of different organs and systems especially the central nervous system, urogenital tract, heart, and lungs. The mandibulofacial defect causes death by respiratory distress. Limb reduction is severe and includes shoulder and pelvis hypoplasia, phocomelia with humerus hypoplasia, absent radius and ulna, complete absence of long bones of the legs, and various hand anomalies, predominantly preaxial reduction. These infants also show facial dysmorphism and ear anomalies. The condition is a rare with an autosomal recessive mode of inheritance. The prognosis is poor and this condition leads to death in utero or shortly after birth. [from SNOMEDCT_US]

MedGen UID:
349730
Concept ID:
C1860119
Disease or Syndrome
4.

Absent forearm

MedGen UID:
278055
Concept ID:
C1408532
Finding; Finding
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