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Items: 6

1.

Baller-Gerold syndrome

Baller-Gerold syndrome (BGS) can be suspected at birth in an infant with craniosynostosis and upper limb abnormality. The coronal suture is most commonly affected; the metopic, lambdoid, and sagittal sutures may also be involved alone or in combination. Upper limb abnormality can include a combination of thumb hypo- or aplasia and radial hypo- or aplasia and may be asymmetric. Malformation or absence of carpal or metacarpal bones has also been described. Skin lesions may appear anytime within the first few years after birth, typically beginning with erythema of the face and extremities and evolving into poikiloderma. Slow growth is apparent in infancy with eventual height and length typically at 4 SD below the mean. [from GeneReviews]

MedGen UID:
120532
Concept ID:
C0265308
Disease or Syndrome
2.

Schinzel phocomelia syndrome

The Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome (AARRS) is a rare autosomal recessive disorder characterized by severe malformations of upper and lower limbs with severely hypoplastic pelvis and abnormal genitalia. The disorder is believed to represent a defect of dorsoventral patterning and outgrowth of limbs (summary by Kantaputra et al., 2010). [from OMIM]

MedGen UID:
336388
Concept ID:
C1848651
Disease or Syndrome
3.

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
4.

Tukel syndrome

MedGen UID:
332153
Concept ID:
C1836217
Disease or Syndrome
5.

Epiphyseal dysplasia, Baumann type

MedGen UID:
322764
Concept ID:
C1835830
Disease or Syndrome
6.

Carpal bone aplasia

Congenital absence of a carpal bone. [from HPO]

MedGen UID:
324464
Concept ID:
C1836219
Finding
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