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1,671 Possible Causes for 3rd-4th Toe Clinodactyly, Duplication or Triplication of Phalanges, Mild to Severe Mental Retardation

Did you mean: 3rd-4th Toe Clinodactyly, Duplication or Triplication of Phalanges, Mild to, Severe Mental Retardation

  • Kleiner Holmes Syndrome

    […] fingers); Bifid terminal phalanges digits 2 and 3; Absent first metatarsal; Brachydactyly; Fifth finger clinodactyly; Syndactyly (often 3rd-4th toes); Hallux valgus; Increased[panelapp.genomicsengland.co.uk] Mental Retardation, with Spasticity and Pigmentary Tapetoretinal Degeneration Sezary's disease Shaheen Syndrome Shaken Baby Syndrome Shapiro Syndrome Sharma Kapoor Ramji[rgd.mcw.edu] Radiographs show broad, shortened, misshapen first metatarsals and may associate incomplete or complete duplication of proximal phalanges and duplication or triplication of[malacards.org]

  • Polysyndactyly

    Left inguinal hernia (operated) Pallor Systemic examination showed pan-systolic murmur at lower left sternal border, (16) generalized hypotonia, (17)severe mental retardation[ispub.com] […] or triplication of phalanges Clinical features from OMIM: 234280 MalaCards organs/tissues related to Hallux Varus and Preaxial Polysyndactyly: 42 Bone Search GEO for disease[malacards.org] Signs & symptoms Clinical features as described in textbook( 1 ) are as follows: Typical features Reduced / absent corpus Callosum Severe mental retardation Seizure Strabismus[ispub.com]

    Missing: 3rd-4th Toe Clinodactyly
  • Profound Mental Retardation

    Based on twin studies, moderate to severe mental retardation does not appear to be familial, but mild mental retardation does.[iq-tests.eu] This section describes the health states of individuals living with mild, moderate, or severe mental retardation.[www150.statcan.gc.ca] Mild to severe mental retardation is a symptom of several hundred single-gene disorders and many chromosomal abnormalities, including small deletions.[iq-tests.eu]

    Missing: 3rd-4th Toe Clinodactyly Duplication or Triplication of Phalanges
  • Mental Retardation

    Based on twin studies, moderate to severe mental retardation does not appear to be familial, but mild mental retardation does.[iq-tests.eu] This section describes the health states of individuals living with mild, moderate, or severe mental retardation.[www150.statcan.gc.ca] Mild to severe mental retardation is a symptom of several hundred single-gene disorders and many chromosomal abnormalities, including small deletions.[iq-tests.eu]

    Missing: 3rd-4th Toe Clinodactyly Duplication or Triplication of Phalanges
  • Hereditary Hyperekplexia

    […] and 4th fingers with synostoses of the corresponding metacarpals and associated single phalanges, syndactyly of the 2nd and 3rd toes and 5th finger clinodactyly.[amp.pharm.mssm.edu] mental retardation and epilepsy.[ncbi.nlm.nih.gov] Syndactyly type 9 Mesoaxial synostotic syndactyly (MSSD) with phalangeal reduction is a novel and distinct form of non-syndromic syndactyly including complete syndactyly of the 3rd[amp.pharm.mssm.edu]

    Missing: Duplication or Triplication of Phalanges
  • Ring Chromosome 7

    […] syndactyly Webbed 3rd-4th toes 0009779 Bifid uvula 0000193 Clinodactyly of the 5th finger Permanent curving of the pinkie finger 0004209 Holoprosencephaly 0001360 Median[rarediseases.info.nih.gov] We report on a boy with ring chromosome 7 who had severe mental retardation, growth failure, microcephaly, cleft lip and palate, café-au-lait spots, nevus flammeus, and genital[ncbi.nlm.nih.gov] Ring 13 syndrome, a congenital abnormality as-sociated with a ring chromosome 13, is character-ized by severe mental retardation, visceral anom-alies, and external deformities[webview.isho.jp]

    Missing: Duplication or Triplication of Phalanges
  • Acrocallosal Syndrome

    Two patients had only mild to moderate mental retardation at the age of 2(1/2) and 4 years, respectively, with surprisingly good speech development.[ncbi.nlm.nih.gov] It is characterised by moderate to severe mental retardation, hypotonia, agenesis of the corpus callosum and preaxial polydactyly involving both feet and the facial features[ncbi.nlm.nih.gov] Typical characteristics of ACLS are hypoplasia/agenesis of corpus callosum, moderate to severe mental retardation, characteristic craniofacial abnormalities, distinctive digital[ncbi.nlm.nih.gov]

    Missing: 3rd-4th Toe Clinodactyly Duplication or Triplication of Phalanges
  • Crossed Polysyndactyly

    Schinzel A, Schmid W (1980): Hallux duplication, postaxial polydac- tyly, absence of the Corpus calilosum, severe mental retardation, and additional anomalies in two unrelated[documentslide.com] […] which attach near the base of the proximal phalanx, sometimes articulating with the metacarpal head; duplication of whole thumb, comprising a metacarpal and two phalanges[myslide.es] Typical characteristics of ACLS are hypoplasia/agenesis of corpus callosum, moderate to severe mental retardation, characteristic craniofacial abnormalities, distinctive digital[wikigenes.org]

    Missing: 3rd-4th Toe Clinodactyly
  • Oculodentodigital Dysplasia

    2nd, 3rd and 4th fingers.The feet revealed syndyctaly of the 2nd to 5th toes and clinodactyly of the great toes.[sajr.org.za] Vertebral anomalies, epibulbar epidermoids, mental retardation, and numerous other anomalies are frequently associated.[icd10data.com] Microcephaly ranges from mild to severe and is often associated with mild to moderate developmental delay and a characteristic facial phenotype with upslanting palpebral fissures[mendelian.co]

    Missing: Duplication or Triplication of Phalanges
  • Mowat-Wilson Syndrome

    Mowat-Wilson syndrome (MWS) is characterized by severe mental retardation with seizures, specific facial dysmorphism, Hirschsprung disease, anomalies of the corpus callosum[ncbi.nlm.nih.gov] The syndrome is characterized by typical facial features, moderate-to-severe mental retardation, epilepsy and variable congenital malformations, including Hirschsprung disease[ncbi.nlm.nih.gov] Mowat-Wilson syndrome is a genetic disorder characterized by a distinct facial appearance, moderate-to-severe mental retardation, microcephaly, agenesis of the corpus callosum[ncbi.nlm.nih.gov]

    Missing: 3rd-4th Toe Clinodactyly Duplication or Triplication of Phalanges