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401 Possible Causes for Disorder of Digit, Narrow Hands, Syndactyly

  • Polydactyly

    What is syndactyly? Syndactyly is the webbing or fusing together of two or more fingers or toes.[] Polydactyly can occur as an isolated disorder (non-syndromic polydactyly) or as a part of an anomaly syndrome (syndromic polydactyly).[] Sometimes the extra digit is connected to the hand or foot with only a narrow piece of tissue.[]

  • Syndactyly

    I believe it advisable to leave the third metacarpal in place and not to narrow the hand by removing it and shifting the index ray ulnarward.[] (disorder), Symphalangy (disorder), Syndactylism, Symphalangism, Congenital webbing of digits, Syndactylus, Syndactyly (disorder), symphalangy, Syndactyly, Symphalangy, Webbing[] This study reports the first frameshift mutation in the BHLHA9 causing mesoaxial synostotic syndactyly and phalangeal reduction.[]

  • Ectrodactyly

    On both of his hands he is missing his second digit (Ectrodactyly) and has a double thumb (Syndactyly) and on both his feet he is also missing his second digit.[] […] and the hand is cleft where the metacarpal of the finger should… It seems that disorders affecting the digits are almost always hereditary and inherited – and likely dominant[] In the past, doctors have typically tried to repair and close the cleft in attempt to give the hand and/or foot a more normal appearance and a narrower shape.[]

  • Saethre-Chotzen Syndrome

    Saethre-Chotzen syndrome (SCS) is a type of acro-cephalo-syndactyly (ACS) syndrome, characterized by premature fusion of the coronal sutures, facial dysmorphism, syndactyly[] Abstract Craniosynostosis (premature fusion of the skull sutures) occurs as a clinically heterogeneous group of disorders, frequently involving digital abnormalities.[] ( dolichocephaly ) [4] Head is short from front to back [5] Lopsided face [4] Low-set hairline causing forehead to appear tall and wide [5] Defects of the hands and feet[]

  • Smith Lemli Opitz Syndrome

    At autopsy the infant had hydrops, unusual face, cleft palate, genital abnormalities, Dandy-Walker malformation, and absence of toe syndactyly.[] Syndrome Ogden syndrome Ohdo syndrome OI/EDS Combined Syndrome OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME An autosomal dominant disorder characterized by delayed psychomotor[] Other dysmorphic features may include microcephaly, ptosis, epicanthal folds, short nasal bridge, bitemporal narrowing, and micrognathia.[]

  • Oculodentodigital Dysplasia

    We observed bilateral syndactyly in 32 patients, with symmetric involvement in 31 of these.[] Oculodentodigital dysplasia (ODDD) (OMIM #164200) is a rare congenital, autosomal dominant disorder comprising craniofacial, ocular, dental, and digital anomalies.[] Abnormalities observed in ODDD affect the eye, dentition, and digits of the hands and feet.[]

  • Craniofrontonasal Dysplasia

    Hand polydactyly Hemihypotrophy of lower limb Preaxial foot polydactyly Sandal gap Toe syndactyly Abnormality of prenatal development or birth Thickened nuchal skin fold[] […] bossing, broad grooved or bifid nasal tip, cleft lip and/or palate, high arched palate), skeletal anomalies (clavicle pseudoarthrosis, coronal craniosynostosis, various digital[] Surgery may also be used to narrow the nose and reduce neck webbing.[]

  • Central Polydactyly of Fingers

    […] differentiation of the fingers and hand plate, duplication, and overgrowth, as well as other generalized anomalies, are then presented in detail, including symbrachydactyly, syndactyly[] The boy’s condition, polydactyly, is a relatively rare genetic disorder. Usually with this condition, the extra digits are on the little finger side of the hand.[] One theory gaining recognition is the role of digital vasoconstriction (narrowing of blood vessels).[]

  • Central Polydactyly of Toes

    synostotic syndactyly with phalangeal reduction (MSSD): syndactyly type IX” Julius Matthias Weinrich & Peter Bannas Skeletal Radiology (2018) Mesoaxial synostotic syndactyly[] The boy’s condition, polydactyly, is a relatively rare genetic disorder. Usually with this condition, the extra digits are on the little finger side of the hand.[] Treatment of Polydactyly If the duplicated small finger is hypoplastic, rudimentary, and attached to the hand by a narrow pedicle it can be removed in the newborn.[]

  • Brachydactyly

    Ophthalmoscopy showed mild narrowing of retinal arteries. Serum electrolytes, blood gases, and renal function were normal.[] Primary hypertrophic osteoarthropathy (PHO), a rare hereditary disorder with digital clubbing, subperiosteal new bone formation, and arthropathy, has been linked mutations[] We compared the findings in our case with those of brachydactyly B, Fuhrmann syndrome and Haas-type syndactyly.[]

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