Create issue ticket

150 Possible Causes for Down Syndrome, Sandal Gap

  • Partial Trisomy 21

    Abstract A case of "atypical" Down Syndrome (DS), where the proposita did not exhibit all of the clinical features of DS and had de novo partial trisomy 21, was studied.[] In addition, children with DS may have a single palmar crease, short hands and fingers, clinodactyly, sandal gap deformity, and plantar furrow.[] Last updated Sept. 13, 2017 The topic Partial Trisomy 21 Down Syndrome you are seeking is a synonym, or alternative name, or is closely related to the medical condition Down[]

  • Mental Retardation

    What is Down syndrome?[] 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[] Mortality rates at an early age have been found to be higher in children suffering from Down syndrome.[]

  • Patau Syndrome

    What is Down syndrome?[] gap : Wide spacing between big toe and the second toe.[] What are Down's, Edwards' and Patau's syndromes? Down's syndrome Down's syndrome causes some level of learning disability. It can vary from mild to severe.[]

  • Down Syndrome

    […] about Down syndrome.[] The space between the first and second toes may also be widened (sandal-gap toes).[] gap”) Small internipple distance Brushfield spots Nuchal skin fold Reliable and discriminative signs Brachycephaly Hypotonia Flat face Upward slant of the eye split Transverse[]

  • Cataract - Congenital Heart Disease - Neural Tube Defect Syndrome

    Down Syndrome Treatment Options and Outlook There are no specific treatments for Down syndrome.[] gap Microdontia Renal hypoplasia/aplasia Bilateral single transverse palmar creases Aganglionic megacolon Hypotrichosis Depressed nasal ridge Type II diabetes mellitus Thick[] gap toe) Widened iliac angle Short ear length Short frontal lobe One of the largest evaluations of routine ultrasonographic examination was the Eurofetus study that analyzed[]

  • X Chromosome Anomaly

    ., Down syndrome) (2) since the additional X chromosome is predominantly inactivated (but the entire X chromosome is not inactivated.) increase in phenotypic severity is seen[] gap what are the following potential medical complications from: heart defect (50%) short stature hypothyroidism myopia & other eye disorders (inc adult cataracts) leukemia[] Down's syndrome The most well-known type of chromosome abnormality is Down's syndrome .[]

  • Nicolaides-Baraitser Syndrome

    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[] Foyle Down Syndrome Trust The Foyle Down Syndrome Trust was formed by local parents of children with Down’s syndrome when they believed that more could be done to develop[]

  • Congenital Abnormality

    Symptoms of down syndrome poster. Abnormal ears, short hands, flattened face and nose, heart disease, big toes widely spaced.[] gap toe) Widened iliac angle Short ear length Short frontal lobe One of the largest evaluations of routine ultrasonographic examination was the Eurofetus study that analyzed[] Down syndrome leads to delays in physical growth and neurodevelopmental disability, and individuals affected by Down syndrome possess characteristic facial features.[]

  • Eye Defects - Arachnodactyly - Cardiopathy Syndrome

    Dysplasia 1 Distal 22q11.2 Microdeletion Syndrome Down Syndrome Duane-Radial Ray Syndrome Dubowitz Syndrome Ectodermal Dysplasia-Intellectual Disability-Central Nervous System[] However, an increased risk of childhood leukemia has been associated with genetic syndromes including Down syndrome, Bloom syndrome, neurofibromatosis, Schwachman syndrome[] […] of Down’s syndrome include small stature, flattened/round faces with an extra fold on the eyelids, saddle nose (a nose in which the bridge has an externally visible concavity[]

  • Pyknodysostosis

    Differential Diagnosis Osteopetrosis Down syndrome Discussion Background Pyknodysostosis is a rare (fewer than 130 cases described) congenital disorder with autosomal recessive[] Figure 1 Toes showing sandal gap deformity . Figure 2 Hands showing short stubby spoon shaped digits with dystrophic nails .[] […] dysplasia, hypothyroidism, hypophosphatasia, otopalatodigital syndrome, primary acroosteolysis (Hajdu-Cheney syndrome), pachydermoperiostosis, progeria, syndrome of Down.[]

Further symptoms

Similar symptoms