Acheiropodia

An extremely rare developmental disorder characterized by bilateral, congenital and complete amputation of the distal extremities (amputation of distal epiphysis of the humerus, distal portion of the tibial diaphysis, aplasia of the radius, ulna, fibula) and aplasia of hands and feet (aplasia of carpal, metacarpal, tarsal, metatarsal and phalangeal bones). Rarely, an ectopic bone can be found at the distal end of the humerus. No other systemic manifestations have been reported and the disorder follows an autosomal recessive pattern of inheritance.



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Narrow down the case reports



Total: 1 (papers)

  


(per page)
Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)
PMID
(PMCID)
1
(43.6%)
11582532
[Femur-fibula-ulna (FFU) complex in the 33rd week of gestation: ultrasonography, radiology, pathology and differential diagnosis. Case report].
Guschmann M, Becker R, Urban M, Entezami M, Hese S, Vogel M.
Klin Padiatr. 2001;213(5):301-5.
Peromelia
Autopsy Differential Diagnosis Females Femur Fetus Fibula Homo sapiens Male Pregnancy Pregnancy Trimester, Third Ultrasonography, Prenatal
        

Phenotype(s) retrieved from Orphanet

    Total: 8

HPO ID Term Frequency
HP:0000944 Abnormality of the metaphysis Very frequent (99-80%)
HP:0002990 Fibular aplasia Very frequent (99-80%)
HP:0003974 Absent radius Very frequent (99-80%)
HP:0003982 Aplasia of the ulna Very frequent (99-80%)
HP:0004050 Absent hand Very frequent (99-80%)
HP:0005792 Short humerus Very frequent (99-80%)
HP:0005930 Abnormality of epiphysis morphology Very frequent (99-80%)
HP:0009813 Upper limb phocomelia Very frequent (99-80%)


Phenotype(s) retrieved from case reports

    Total: 1

HPO ID Term # of case reports
HP:0025410 Splenogonadal fusion 1


Causative gene(s) retrieved from Orphanet

    Total: 1

Gene Symbol Gene Name Entrez Gene ID
LMBR1 limb development membrane protein 1 64327