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Results: 5

1.

Intrauterine growth retardation

MedGen UID:
342890
Concept ID:
C1853481
Finding
2.

Severe

A term used to describe cells that look abnormal under a microscope. These cells are more likely to grow and spread quickly than cells in low-grade cancer or in growths that may become cancer. [from NCI]

MedGen UID:
104640
Concept ID:
C0205082
3.

Intrauterine growth restriction

abnormal fetal physical growth or growth potential at any gestational stage. [from CRISP]

MedGen UID:
4693
Concept ID:
C0015934
Pathologic Function
4.

Placental insufficiency

Failure of the PLACENTA to deliver an adequate supply of nutrients and OXYGEN to the FETUS. [from MeSH]

MedGen UID:
45942
Concept ID:
C0032051
Disease or Syndrome
5.

Atelosteogenesis type 1

The FLNB-related disorders include a spectrum of phenotypes ranging from mild (spondylocarpotarsal synostosis [SCT] syndrome and Larsen syndrome) to severe (atelosteogenesis types I [AOI] and III [AOIII], boomerang dysplasia). SCT syndrome is characterized by disproportionate short stature, block vertebrae, scoliosis and lordosis, carpal and tarsal fusion, club feet, hearing loss, dental enamel hypoplasia, and mild facial dysmorphisms. Larsen syndrome is characterized by congenital dislocations of the hip, knee, and elbow; club feet (equinovarus or equinovalgus foot deformities); scoliosis and cervical kyphosis, which can be associated with a cervical myelopathy; short, broad, spatulate distal phalanges; and distinctive craniofacies (prominent forehead, depressed nasal bridge, malar flattening, andwidely spaced eyes). Both can have midline cleft palate and conductive hearing loss. AOIII and AOI are characterized by severe short-limbed dwarfism; dislocated hips, knees, and elbows; and club feet. AOI is lethal in the perinatal period. [from GeneReviews]

MedGen UID:
82701
Concept ID:
C0265283
Congenital Abnormality

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