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46 Possible Causes for Muscle Hypotonia, Sandal Gap

  • Craniofrontonasal Dysplasia

    gap Scoliosis Sensorineural hearing impairment Sprengel anomaly Thickened nuchal skin fold Woolly hair Aplasia / Hypoplasia of the corpus callosum Aplasia / Hypoplasia of[] Some individuals affected by CFND may also have diminished muscle tone (hypotonia), developmental delays, hearing impairment (sensorineural deafness), a sunken chest (pectus[] Low or weak muscle tone 0001252 Oral cleft Cleft of the mouth 0000202 Plagiocephaly Flat head syndrome Flattening of skull Rhomboid shaped skull [ more ] 0001357 Sandal gap[]

  • Dubowitz Syndrome

    gap Gap between 1st and 2nd toes Gap between first and second toe Increased space between first and second toes Sandal gap between first and second toes Wide space between[] Low or weak muscle tone 0001252 Neuroblastoma 0003006 Otitis media Middle ear infection 0000388 Pes planus Flat feet Flat foot [ more ] 0001763 Short attention span Poor[] muscles) is also a frequent finding.[]

  • Weaver Syndrome

    gap Gap between 1st and 2nd toes Gap between first and second toe Increased space between first and second toes Sandal gap between first and second toes Wide space between[] Other common symptoms include hypertonia (increased muscle tone, tight muscles) as well as hypotonia (decreased muscle tone, "floppy" muscles) and a hoarse low-pitched cry[] Other symptoms include diminished muscle tone (hypotonia), muscle weakness, hernias in the abdomen (umbilical hernias), and/or mental retardation.[]

  • Wolf Hirschhorn Syndrome

    […] between first and second toes (sandal gap), short stature GI : duodenal and anorectal atresia, umbilical hernia [] Jaw & Teeth Periodontitis At the beginning[] Generalized muscle hypotonia was observed at birth.[] hypotonia, seizures, and congenital heart defects.[]

  • Short Stature - Optic Atrophy - Pelger-Huët Anomaly Syndrome

    […] nerve atrophy, and pelger-huet anomaly may include: Pelger-Huet anomaly Short Stature Brachycephaly Epicanthus Hypertelorism Proptosis Thin vermilion border Brachydactyly Sandal[] gap Single transverse palmar crease Syndactyly Cutis laxa Congenital eye abnormality Hypermetropia Myopia Optic atrophy Strabismus Micromelia • • • Back to: « Short stature[]

  • Cap Myopathy

    He shows sandal gaps on both flat feet with clinodactyly of the fourth and fifth toes (and more) 612513 PMID: 22579565 severe developmental delay, congenital microcephaly,[] People with cap myopathy have muscle weakness (myopathy) and poor muscle tone (hypotonia) throughout the body, but they are most severely affected in the muscles of the face[] Genetics Home Reference : 25 Cap myopathy is a disorder that primarily affects skeletal muscles, which are muscles that the body uses for movement.[]

  • Congenital Cataract-Hearing Loss-Severe Developmental Delay Syndrome

    A bigger than normal space between the first and second toe (the 'sandal gap'). Muscles that lack tone and can be quite floppy (this is often most noticeable in babies).[] Muscle tone vs. muscle strength The low muscle tone associated with hypotonia must not be confused with low muscle strength.[] Additional findings may occur in some cases including diminished muscle tone (hypotonia), abnormally long, slender fingers (arachnodactyly), flat feet (pes planus), and osteochondritis[]

  • Tenorio Syndrome

    gap and neurological manifestations such as epilepsy have been reported.[] […] atrophy Mitral valve prolapse Hydrocephalus Raynaud phenomenon Arrhythmia Aortic regurgitation Mask-like facies Neonatal hypotonia Cerebral cortical atrophy Cerebral palsy[] Occasionally, cranial asymmetry, emimegalencephaly, dysgenesis of the corpus callosus, ptosis, horizontal nystagmus, bilateral cataracts, wide feet and hands, macrodactyly, wide sandal[]

  • Down Syndrome

    The space between the first and second toes may also be widened (sandal-gap toes).[] From Wikidata Jump to navigation Jump to search chromosomal disease characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused[] gap”) Small internipple distance Brushfield spots Nuchal skin fold Reliable and discriminative signs Brachycephaly Hypotonia Flat face Upward slant of the eye split Transverse[]

  • X-Linked Mental Retardation 93

    The marfanoid features include a tall stature, long thin hyper-extensible fingers and toes, but no true arachnodactyly, short halluces, long second toes and sandal gap [ 4[]

Further symptoms

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