Create issue ticket

52 Possible Causes for Partial Syndactyly of Fingers and Toes, Short Stature in Children

  • 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[] In addition to fused sutures, children with Saethre Chotzen syndrome also have a characteristic low-set hairline, a “beaked” nose and short stature.[] […] skin syndactyly between the finger) and the patients demonstrated triangular hypertrophied great toes with valgus deformity (contrary to Pfeiffer syndrome).[]

  • Cornelia De Lange Syndrome

    […] clinodactyly (curved 5th finger) Abnormal palmar crease Radial head dislocation/abnormal elbow extension Short 1st metacarpal/proximally placed thumb Bunion Partial 2,3 syndactyly[] Cornelia de Lange Syndrome Definition [ edit ] Cornelia de Lange Syndrome is a rare developmental malformation syndrome characterized by mental retardation, short stature,[] (webbing between 2nd and 3rd toes) Scoliosis (curvature of the spine) Pectus excavatum (chest or sternum deformity) Hip dislocation or dysplasia Neurosensory/Skin: Ptosis[]

  • Cri Du Chat Syndrome

    Syndactyly (partial webbing or fusing of fingers or toes). Simian crease (single palmar crease).[] Babies Characteristic high pitched cry at birth Low birth weight Poor muscle tone Developmental delay Small head Round "moon" face Children Small thin build and short stature[] Typical facial features - small chin, long nose, which don't look particularly odd, but the children look as if they are related.[]

  • Syndactyly

    Syndactyly A fusion of two or more toes or fingers. syndactyly partial/total webbing of some/all digits, due to soft-tissue and/or bone fusion across adjacent interdigital[] Low birth weight and slow postnatal growth rates are usually result in short stature. The hair is often sparse and light-colored.[] In early human fetal development, webbing (syndactyly) of the toes and fingers is normal.[]

  • 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[] Skeletal anomalies such as short stature, high palate, craniosynostosis, scoliosis, pes planus, hand contractures, and joint hypermobility have been reported.[] Infants and young children may have feeding difficulties but may later develop constipation or diarrhea.[]

  • Aarskog-Scott Syndrome

    Pectus carinatum with excavatum was noticed, along with brachydactyly, bilateral fifth finger clinodactyly, bilateral partial syndactyly of the second and third toes, interdigital[] Abstract Aarskog syndrome is a familial condition associated with craniofacial anomalies, genital malformations and short stature.[] Shawl scrotum in children with short stature is characteristic of Aarskog syndrome but may not be seen in 20% cases.[]

  • Weismann Netter Syndrome

    syndactyly of fingers and toes, brachydactyly of toes, valgus deformity of hypertrophied triangular great toes, broad phalanges of the great toes and broad first metatarsals[] In 1954, Weismann-Netter and Stuhl described three sporadic adults and a mother and her three children with short stature and congenital anterior bowing of lower legs [Weismann-Netter[] The medical definition states that short stature is two standard deviations or more below the mean for children of the same age and gender.[]

  • Acrocephaly

    Apert syndrome is also characterized by partial to complete fusion (syndactyly) of certain fingers and toes (digits).[] Short stature and no physiologic spinal curvature are observed. Children are straight as a reed. Refer to the following images.[] In addition, finger joints tend to become stiff by about four years of age. Syndactyly also typically involves the second, third, and fourth toes.[]

  • Micrognathism

    […] soft tissue syndactyly of the fingers and toes involving interdigital spaces 2 to 4, and bilateral talipes equinovarus.[] This syndrome is characterized by facial dysmorphism, congenital heart defects, short stature and also a wide phenotypic variation.[] University of Londrina (HU-UEL) – Londrina (PR), Brazil ABSTRACT Noonan Syndrome is one of the most common genetic syndromes and also an important differential diagnosis in children[]

  • Apert Syndrome

    Other signs were represented by syndactyly involving partial fusion of the fingers and toes. Also, mild mental deficiency was recorded.[] Children with Apert syndrome may have mental deficiencies, short stature, hearing impairment, frequent ear infections, prominent and/or bulging eyes, a large or late-closing[] Apert syndrome is also characterized by partial to complete fusion (syndactyly) of certain fingers and toes (digits).[]

Further symptoms