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137 Possible Causes for Mental Retardation, Partial Syndactyly of Fingers and Toes

  • Saethre-Chotzen Syndrome

    Unilateral or bilateral coronal synostosis, low frontal hair line, strabismus, ptosis, and partial cutaneous syndactyly of fingers and toes are findings suggestive of the[] Strikingly, all these patients were severely mentally retarded, which is otherwise a rare finding in Saethre-Chotzen syndrome.[] […] skin syndactyly between the finger) and the patients demonstrated triangular hypertrophied great toes with valgus deformity (contrary to Pfeiffer syndrome).[]

  • Hypertelorism

    Limb manifestations consist of splitting of nails (40%), broad great toes, partial syndactyly of fingers and toes, hy-perextensible joints, short 5th fingers, clinodactyly[] The phenotype of the patients is different from that of all other previously described types of X-linked mental retardation (XLMR).[] retardation and seizures.[]

  • Apert Syndrome

    Other signs were represented by syndactyly involving partial fusion of the fingers and toes. Also, mild mental deficiency was recorded.[] Andere Ausgaben - Alle anzeigen Medical aspects of mental retardation Charles H.[] Apert syndrome is also characterized by partial to complete fusion (syndactyly) of certain fingers and toes (digits).[]

  • Laurence Moon Syndrome

    Nine patients (8%) showed syndactyly; this was usually partial, most commonly involving the second and third toes.[] Laurence-Moon-Biedl syndrome [ law rens mo̳n be d'l ] a hereditary autosomal recessive syndrome characterized by obesity, hypogenitalism, retinitis pigmentosa, mental retardation[] Lau·rence-Moon syn·drome ( law'rĕnts mūn ), [MIM*245800] disorder characterized by mental retardation, pigmentary retinopathy, hypogenitalism, and spastic paraplegia; autosomal[]

  • Acrocallosal Syndrome

    He also had 2/3 partial cutaneous syndactyly on the right and 3/4 partial cutaneous syndactyly on the left.[] retardation.[] Jump to search syndrome that is an autosomal recessive disorder, which is characterized by corpus callosum agenesis, polydactyly, multiple dysmorphic features, motor and mental[]

  • Lenz-Majewski Syndrome

    In severe cases, the fingers, toes, hands, feet, and/or lower legs may be partially or completely absent.[] Characterized by multiple congenital anomalies (delayed closure of fontanel, proximal symphalangism, prominent scalp cutaneous veins), mental retardation, and progressive[] Lenz-Majewski syndrome - congenital anomalies, mental retardation, sclerosis of the skeletal system.[]

  • Otoonychoperoneal Syndrome

    syndactyly of fingers and toes, brachydactyly of toes, valgus def[] […] c MNT280 Mental Retardation, Autosomal Dominant 43 27 2196 c MNT213 Mental Retardation, Autosomal Recessive 40 27 2197 c MNT222 Mental Retardation, Autosomal Dominant 29 27[] syndactyly Talipes equinovarus Toe syndactyly Severe muscular hypotonia Chorioretinal coloboma Plagiocephaly Proximal placement of thumb Abnormal vertebral morphology High[]

  • Fraser Syndrome

    Some of the most common ones are middle and outer ear deformities, partial fusion of the fingers and toes (syndactyly), complete fusion of the eyelids (cryptophthalmos) and[] The patient had microphthalmia, blindness, widely spaced nipples, bifid ureter, syndactyly of the toes, and mental retardation.[] Congenital malformations of the nose, ears, larynx and renal system, as well as mental retardation, manifest occasionally.[]

  • Patel-Bixler Syndrome

    syndactyly of fingers and toes.[] Colobomatous microphthalmia, heart disease, hearing loss, and mental retardation: a syndrome. J Pediatr Ophthalmol Strabismus. 1979;16:122-128.[] There is mental retardation, midfacial hypoplasia, small nose, hypertelorism, ptosis, and blepharophimosis.[]

  • Autosomal Dominant Mental Retardation Type 21

    syndactyly of fingers and toes; Brachymesophalangy of hands and feet; [Feet]; Broad great toe NEUROLOGIC: [Central nervous system]; Occasional mental retardation; Hydrocephalus[] Mental Retardation Definition Mental retardation is a developmental disability that first appears in children under the age of 18.[] Retardation; 1p-deletion, Williams, Smith-Magenis, Miller-Dieker, DiGeorge, Prader-Willi, Alagille, Saethre-Chotzen, Sotos Various P064 Mental retardation, x-linked (XLMR[]

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