Constriction rings syndrome

Constriction rings syndrome is a congenital limb malformation disorder with an extremely variable clinical presentation characterized by the presence of partial to complete, congenital, fibrous, circumferential, constriction bands/rings on any part of the body, although a particular predilection for the upper or lower extremities is seen. Phenotypes range from only a mild skin indentation to complete amputation of parts of the fetus (e.g. digits, distal limb). Compression from the rings may lead to edema, skeletal anomalies (e.g. fractures, foot deformities) and, infrequently, neural compromise.



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Narrow down the case reports



Total: 107 (papers)

  


(per page)
Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)
PMID
(PMCID)
71
(4.0%)
4054420
Placental teratoma or acardius amorphus with amniotic band syndrome.
Calame JJ, van der Harten JJ.
Eur J Obstet Gynecol Reprod Biol. 1985;20(4):265-73.
Teratoma
Abnormality, Severe Teratoid Adult Amniotic Band Syndrome Congenital Heart Defects Differential Diagnosis Females Homo sapiens Placenta Disorders Pregnancy Pregnancy Complications, Neoplastic Rupture, Spontaneous Teratoma
71
(4.0%)
4050333
The amniotic band syndrome as a cause of anencephaly. Report of a case.
Urich H, Herrick MK.
Acta Neuropathol. 1985;67(3-4):190-4.
Anencephaly
Amniotic Band Syndrome Anencephaly Central Nervous System Eye Females Homo sapiens Infant, Newborn
71
(4.0%)
3320375
Amniotic band syndrome in a rhesus monkey: a case report.
Tarantal AF, Hendrickx AG.
J Med Primatol. 1987;16(5):291-9.
Hydrocephalus
Amniotic Band Syndrome Animals Females Homo sapiens Infant, Newborn Macaca mulatta Monkey Diseases Pregnancy Ultrasonography
71
(4.0%)
2776956
Solitary thick intra-uterine membranes not associated with the amniotic band syndrome; three case reports.
Zosmer A, Shoham Z, Dgani R, Ashkenazi M, Levin J, Lancet M.
Eur J Obstet Gynecol Reprod Biol. 1989;32(2):173-8.
Hypospadias
Adult Amniotic Band Syndrome Females Homo sapiens Infant, Newborn Male Placenta Pregnancy Uterus
71
(4.0%)
2655354
[Amniotic band syndrome with anencephaly--a case report].
Yilmazturk A, Schluter W.
Zentralbl Gynakol. 1989;111(3):173-7.
Anencephaly
Adrenal Glands Adult Amniotic Band Syndrome Anencephaly Females Fetal Membranes, Premature Rupture Homo sapiens Infant, Newborn Limb Deformities, Congenital Pregnancy Pregnancy Trimester, Second Ultrasonography
71
(4.0%)
1919974
Chorioretinal lacuna in the amniotic band syndrome.
Hashemi K, Traboulsi EI, Chavis R, Scribanu N, Chrousos GA.
J Pediatr Ophthalmol Strabismus. 1991;28(4):238-9.
Hypertelorism
Amniotic Band Syndrome Brain Choroid Females Homo sapiens Infant, Newborn Retina
71
(4.0%)
1477047
A case of amniotic band syndrome with bilateral epibulbar choristoma.
Murata T, Hashimoto S, Ishibashi T, Inomata H, Sueishi K.
Br J Ophthalmol. 1992;76(11):685-7.
Oligohydramnios
Adult Amniotic Band Syndrome Connective Tissue Ectopic Tissue Eye Eye Neoplasms Females Homo sapiens Infant, Newborn
        

Phenotype(s) retrieved from Orphanet

    Total: 0

HPO ID Term Frequency


Phenotype(s) retrieved from case reports

    Total: 41

HPO ID Term # of case reports
HP:0002323 Anencephaly 6
HP:0001159 Syndactyly 5
HP:0002084 Encephalocele 4
HP:0030716 Acrania 4
HP:0002435 Meningocele 3
HP:0030769 Exencephaly 3
HP:0001562 Oligohydramnios 2
HP:0002650 Scoliosis 2
HP:0005864 Pseudoarthrosis 2
HP:0010866 Abdominal wall defect 2
HP:0100699 Scarring 2
HP:0100758 Gangrene 2
HP:0000201 Pierre-Robin sequence 1
HP:0000252 Microcephaly 1
HP:0000486 Strabismus 1
HP:0000508 Ptosis 1
HP:0000528 Anophthalmia 1
HP:0000568 Microphthalmia 1
HP:0000589 Coloboma 1
HP:0000969 Edema 1
HP:0001171 Split hand 1
HP:0001289 Confusion 1
HP:0001839 Split foot 1
HP:0001883 Talipes 1
HP:0002119 Ventriculomegaly 1
HP:0002144 Tethered cord 1
HP:0002414 Spina bifida 1
HP:0002617 Dilatation 1
HP:0003422 Vertebral segmentation defect 1
HP:0003980 Pseudarthrosis of the radius 1
HP:0007858 Chorioretinal lacunae 1
HP:0009792 Teratoma 1
HP:0010442 Polydactyly 1
HP:0010878 Fetal cystic hygroma 1
HP:0012032 Lipoma 1
HP:0030779 Ethmocephaly 1
HP:0030855 Anterior staphyloma 1
HP:0100258 Preaxial polydactyly 1
HP:0100259 Postaxial polydactyly 1
HP:0100537 Fasciitis 1
HP:0410030 Cleft lip 1


Causative gene(s) retrieved from Orphanet

    Total: 0

Gene Symbol Gene Name Entrez Gene ID