Arthrogryposis (English Wikipedia)

Kalampokas E, Kalampokas T, Sofoudis C, Deligeoroglou E, Botsis D (2012). "Diagnosing arthrogryposis multiplex congenita: a review". ISRN Obstetrics and Gynecology. 2012: 264918. doi:10.5402/2012/264918. PMC 3461621. PMID 23050160.
Bamshad M, Van Heest AE, Pleasure D (July 2009). "Arthrogryposis: a review and update". The Journal of Bone and Joint Surgery. American Volume. 91 (Suppl 4): 40–6. doi:10.2106/JBJS.I.00281. PMC 2698792. PMID 19571066.
Bevan WP, Hall JG, Bamshad M, Staheli LT, Jaffe KM, Song K (2007). "Arthrogryposis multiplex congenita (amyoplasia): an orthopaedic perspective". Journal of Pediatric Orthopedics. 27 (5): 594–600. doi:10.1097/BPO.0b013e318070cc76. PMID 17585274.
Miller M, Dobbs MB (October 2015). "Congenital Vertical Talus: Etiology and Management". The Journal of the American Academy of Orthopaedic Surgeons. 23 (10): 604–11. doi:10.5435/JAAOS-D-14-00034. PMID 26337950. S2CID 2282828.
Fassier A, Wicart P, Dubousset J, Seringe R (October 2009). "Arthrogryposis multiplex congenita. Long-term follow-up from birth until skeletal maturity". Journal of Children's Orthopaedics. 3 (5): 383–90. doi:10.1007/s11832-009-0187-4. PMC 2758174. PMID 19669823.
Brooks JG, Coster DJ (May 1994). "Arthrogryposis multiplex congenita: a report of two cases". Australian and New Zealand Journal of Ophthalmology. 22 (2): 127–32. doi:10.1111/j.1442-9071.1994.tb00780.x. PMID 7917267.
Wynne-Davies R, Williams PF, O'Connor JC (February 1981). "The 1960s epidemic of arthrogryposis multiplex congenita: a survey from the United Kingdom, Australia and the United States of America". The Journal of Bone and Joint Surgery. British Volume. 63-B (1): 76–82. doi:10.1302/0301-620X.63B1.7204479. PMID 7204479.
Rink BD (June 2011). "Arthrogryposis: a review and approach to prenatal diagnosis". Obstetrical & Gynecological Survey. 66 (6): 369–77. doi:10.1097/OGX.0b013e31822bf5bb. PMID 21851751. S2CID 34468857.
Smit LM, Barth PG (June 1980). "Arthrogryposis multiplex congenita due to congenital myasthenia". Developmental Medicine and Child Neurology. 22 (3): 371–4. doi:10.1111/j.1469-8749.1980.tb03718.x. PMID 6446471. S2CID 39261871.
Banker BQ, Victor M, Adams RD (September 1957). "Arthrogryposis multiplex due to congenital muscular dystrophy". Brain. 80 (3): 319–34. doi:10.1093/brain/80.3.319. PMID 13471804.
Kizilates SU, Talim B, Sel K, Köse G, Caglar M (March 2005). "Severe lethal spinal muscular atrophy variant with arthrogryposis". Pediatric Neurology. 32 (3): 201–4. doi:10.1016/j.pediatrneurol.2004.10.003. PMID 15730903. INIST 16634238.
Leichtman LG, Say B, Barber N (May 1980). "Primary pulmonary hypoplasia and arthrogryposis multiplex congenita". The Journal of Pediatrics. 96 (5): 950–1. doi:10.1016/S0022-3476(80)80591-9. PMID 7365612.
Illum N, Reske-Nielsen E, Skovby F, Askjaer SA, Bernsen A (November 1988). "Lethal autosomal recessive arthrogryposis multiplex congenita with whistling face and calcifications of the nervous system". Neuropediatrics. 19 (4): 186–92. doi:10.1055/s-2008-1052443. PMID 3205375. S2CID 260242391.
Tiemann, Christian; Bührer, Christoph; Burwinkel, Barbara; Wirtenberger, Michael; Hoehn, Thomas; Hübner, Christoph; van Landeghem, Frank; Stoltenburg-Didinger, Gisela; Obladen, Michael (2005-08-30). "Arthrogryposis multiplex with deafness, inguinal hernias, and early death: A family report of a probably autosomal recessive trait". American Journal of Medical Genetics. Part A. 137 (2): 125–129. doi:10.1002/ajmg.a.30860. PMID 16059941. S2CID 41345689.
Schrander-Stumpel CT, Höweler CJ, Reekers AD, De Smet NM, Hall JG, Fryns JP (January 1993). "Arthrogryposis, ophthalmoplegia, and retinopathy: confirmation of a new type of arthrogryposis". Journal of Medical Genetics. 30 (1): 78–80. doi:10.1136/jmg.30.1.78. PMC 1016242. PMID 8423615.
Di Rocco M, Callea F, Pollice B, Faraci M, Campiani F, Borrone C (October 1995). "Arthrogryposis, renal dysfunction and cholestasis syndrome: report of five patients from three Italian families". European Journal of Pediatrics. 154 (10): 835–9. doi:10.1007/BF01959793. PMID 8529684. S2CID 32845371.
Binkiewicz-Glinska A, Sobierajska-Rek A, Bakula S, Wierzba J, Drewek K, Kowalski IM, Zaborowska-Sapeta K (November 2013). "Arthrogryposis in infancy, multidisciplinary approach: case report". BMC Pediatrics. 13 (1): 184. doi:10.1186/1471-2431-13-184. PMC 3833971. PMID 24215600.
Rahman T, Sample W, Jayakumar S, King MM, Wee JY, Seliktar R, et al. (2006). "Passive exoskeletons for assisting limb movement". Journal of Rehabilitation Research and Development. 43 (5): 583–90. doi:10.1682/JRRD.2005.04.0070. PMID 17123200.
Van Heest AE, Rodriguez R (February 2013). "Dorsal carpal wedge osteotomy in the arthrogrypotic wrist". The Journal of Hand Surgery. 38 (2): 265–70. doi:10.1016/j.jhsa.2012.10.034. PMID 23267756.
Ezaki M, Oishi SN (March 2010). "Index rotation flap for palmar thumb release in arthrogryposis". Techniques in Hand & Upper Extremity Surgery. 14 (1): 38–40. doi:10.1097/BTH.0b013e3181d44583. PMID 20216051.
Matar HE, Beirne P, Garg N (February 2016). "The effectiveness of the Ponseti method for treating clubfoot associated with arthrogryposis: up to 8 years follow-up". Journal of Children's Orthopaedics. 10 (1): 15–8. doi:10.1007/s11832-016-0712-1. PMC 4763152. PMID 26833334.
Machida J, Inaba Y, Nakamura N (March 2017). "Management of foot deformity in children". Journal of Orthopaedic Science. 22 (2): 175–183. doi:10.1016/j.jos.2016.12.009. PMID 28081930.
El-Sobky TA, Samir S, Mahmoud S (July 2020). "Naviculectomy for two ambulatory children with intractable congenital vertical talus: redefining the indications of an old technique". Journal of Pediatric Orthopedics. Part B. 29 (4): 387–391. doi:10.1097/BPB.0000000000000663. PMC 7255489. PMID 31356503.
Hoff JM, Loane M, Gilhus NE, Rasmussen S, Daltveit AK (December 2011). "Arthrogryposis multiplexa congenita: an epidemiologic study of nearly 9 million births in 24 EUROCAT registers". European Journal of Obstetrics, Gynecology, and Reproductive Biology. 159 (2): 347–50. doi:10.1016/j.ejogrb.2011.09.027. PMID 22005589.

inist.fr

pascal-francis.inist.fr

Kizilates SU, Talim B, Sel K, Köse G, Caglar M (March 2005). "Severe lethal spinal muscular atrophy variant with arthrogryposis". Pediatric Neurology. 32 (3): 201–4. doi:10.1016/j.pediatrneurol.2004.10.003. PMID 15730903. INIST 16634238.

medinet.lk

"Arthrogryposis multiplex congenita distal type II associated with facial abnormality". Archived from the original on 2007-09-27. Retrieved 2007-04-25.

newsworks.org

Chen E (27 January 2016). "Building functional, fashionable exoskeletons for babies". NewsWorks The Pulse. Archived from the original on 4 August 2017. Retrieved 10 May 2017.

nih.gov

pubmed.ncbi.nlm.nih.gov

Kalampokas E, Kalampokas T, Sofoudis C, Deligeoroglou E, Botsis D (2012). "Diagnosing arthrogryposis multiplex congenita: a review". ISRN Obstetrics and Gynecology. 2012: 264918. doi:10.5402/2012/264918. PMC 3461621. PMID 23050160.
Bamshad M, Van Heest AE, Pleasure D (July 2009). "Arthrogryposis: a review and update". The Journal of Bone and Joint Surgery. American Volume. 91 (Suppl 4): 40–6. doi:10.2106/JBJS.I.00281. PMC 2698792. PMID 19571066.
Bevan WP, Hall JG, Bamshad M, Staheli LT, Jaffe KM, Song K (2007). "Arthrogryposis multiplex congenita (amyoplasia): an orthopaedic perspective". Journal of Pediatric Orthopedics. 27 (5): 594–600. doi:10.1097/BPO.0b013e318070cc76. PMID 17585274.
Miller M, Dobbs MB (October 2015). "Congenital Vertical Talus: Etiology and Management". The Journal of the American Academy of Orthopaedic Surgeons. 23 (10): 604–11. doi:10.5435/JAAOS-D-14-00034. PMID 26337950. S2CID 2282828.
Fassier A, Wicart P, Dubousset J, Seringe R (October 2009). "Arthrogryposis multiplex congenita. Long-term follow-up from birth until skeletal maturity". Journal of Children's Orthopaedics. 3 (5): 383–90. doi:10.1007/s11832-009-0187-4. PMC 2758174. PMID 19669823.
Brooks JG, Coster DJ (May 1994). "Arthrogryposis multiplex congenita: a report of two cases". Australian and New Zealand Journal of Ophthalmology. 22 (2): 127–32. doi:10.1111/j.1442-9071.1994.tb00780.x. PMID 7917267.
Wynne-Davies R, Williams PF, O'Connor JC (February 1981). "The 1960s epidemic of arthrogryposis multiplex congenita: a survey from the United Kingdom, Australia and the United States of America". The Journal of Bone and Joint Surgery. British Volume. 63-B (1): 76–82. doi:10.1302/0301-620X.63B1.7204479. PMID 7204479.
Rink BD (June 2011). "Arthrogryposis: a review and approach to prenatal diagnosis". Obstetrical & Gynecological Survey. 66 (6): 369–77. doi:10.1097/OGX.0b013e31822bf5bb. PMID 21851751. S2CID 34468857.
Smit LM, Barth PG (June 1980). "Arthrogryposis multiplex congenita due to congenital myasthenia". Developmental Medicine and Child Neurology. 22 (3): 371–4. doi:10.1111/j.1469-8749.1980.tb03718.x. PMID 6446471. S2CID 39261871.
Banker BQ, Victor M, Adams RD (September 1957). "Arthrogryposis multiplex due to congenital muscular dystrophy". Brain. 80 (3): 319–34. doi:10.1093/brain/80.3.319. PMID 13471804.
Stoll C, Alembik Y, Finck S, Janser B (1992). "Arthrogryposis, ectodermal dysplasia and other anomalies in two sisters". Genetic Counseling. 3 (1): 35–9. PMID 1590979.
Kizilates SU, Talim B, Sel K, Köse G, Caglar M (March 2005). "Severe lethal spinal muscular atrophy variant with arthrogryposis". Pediatric Neurology. 32 (3): 201–4. doi:10.1016/j.pediatrneurol.2004.10.003. PMID 15730903. INIST 16634238.
Leichtman LG, Say B, Barber N (May 1980). "Primary pulmonary hypoplasia and arthrogryposis multiplex congenita". The Journal of Pediatrics. 96 (5): 950–1. doi:10.1016/S0022-3476(80)80591-9. PMID 7365612.
Illum N, Reske-Nielsen E, Skovby F, Askjaer SA, Bernsen A (November 1988). "Lethal autosomal recessive arthrogryposis multiplex congenita with whistling face and calcifications of the nervous system". Neuropediatrics. 19 (4): 186–92. doi:10.1055/s-2008-1052443. PMID 3205375. S2CID 260242391.
Tiemann, Christian; Bührer, Christoph; Burwinkel, Barbara; Wirtenberger, Michael; Hoehn, Thomas; Hübner, Christoph; van Landeghem, Frank; Stoltenburg-Didinger, Gisela; Obladen, Michael (2005-08-30). "Arthrogryposis multiplex with deafness, inguinal hernias, and early death: A family report of a probably autosomal recessive trait". American Journal of Medical Genetics. Part A. 137 (2): 125–129. doi:10.1002/ajmg.a.30860. PMID 16059941. S2CID 41345689.
Schrander-Stumpel CT, Höweler CJ, Reekers AD, De Smet NM, Hall JG, Fryns JP (January 1993). "Arthrogryposis, ophthalmoplegia, and retinopathy: confirmation of a new type of arthrogryposis". Journal of Medical Genetics. 30 (1): 78–80. doi:10.1136/jmg.30.1.78. PMC 1016242. PMID 8423615.
Di Rocco M, Callea F, Pollice B, Faraci M, Campiani F, Borrone C (October 1995). "Arthrogryposis, renal dysfunction and cholestasis syndrome: report of five patients from three Italian families". European Journal of Pediatrics. 154 (10): 835–9. doi:10.1007/BF01959793. PMID 8529684. S2CID 32845371.
Binkiewicz-Glinska A, Sobierajska-Rek A, Bakula S, Wierzba J, Drewek K, Kowalski IM, Zaborowska-Sapeta K (November 2013). "Arthrogryposis in infancy, multidisciplinary approach: case report". BMC Pediatrics. 13 (1): 184. doi:10.1186/1471-2431-13-184. PMC 3833971. PMID 24215600.
Rahman T, Sample W, Jayakumar S, King MM, Wee JY, Seliktar R, et al. (2006). "Passive exoskeletons for assisting limb movement". Journal of Rehabilitation Research and Development. 43 (5): 583–90. doi:10.1682/JRRD.2005.04.0070. PMID 17123200.
Van Heest AE, Rodriguez R (February 2013). "Dorsal carpal wedge osteotomy in the arthrogrypotic wrist". The Journal of Hand Surgery. 38 (2): 265–70. doi:10.1016/j.jhsa.2012.10.034. PMID 23267756.
Ezaki M, Oishi SN (March 2010). "Index rotation flap for palmar thumb release in arthrogryposis". Techniques in Hand & Upper Extremity Surgery. 14 (1): 38–40. doi:10.1097/BTH.0b013e3181d44583. PMID 20216051.
Matar HE, Beirne P, Garg N (February 2016). "The effectiveness of the Ponseti method for treating clubfoot associated with arthrogryposis: up to 8 years follow-up". Journal of Children's Orthopaedics. 10 (1): 15–8. doi:10.1007/s11832-016-0712-1. PMC 4763152. PMID 26833334.
Machida J, Inaba Y, Nakamura N (March 2017). "Management of foot deformity in children". Journal of Orthopaedic Science. 22 (2): 175–183. doi:10.1016/j.jos.2016.12.009. PMID 28081930.
El-Sobky TA, Samir S, Mahmoud S (July 2020). "Naviculectomy for two ambulatory children with intractable congenital vertical talus: redefining the indications of an old technique". Journal of Pediatric Orthopedics. Part B. 29 (4): 387–391. doi:10.1097/BPB.0000000000000663. PMC 7255489. PMID 31356503.
Hoff JM, Loane M, Gilhus NE, Rasmussen S, Daltveit AK (December 2011). "Arthrogryposis multiplexa congenita: an epidemiologic study of nearly 9 million births in 24 EUROCAT registers". European Journal of Obstetrics, Gynecology, and Reproductive Biology. 159 (2): 347–50. doi:10.1016/j.ejogrb.2011.09.027. PMID 22005589.

rarediseases.info.nih.gov

Arthrogryposis and ectodermal dysplasia at NIH's Office of Rare Diseases
Arthrogryposis IUGR thoracic dystrophy at NIH's Office of Rare Diseases
Arthrogryposis-like hand anomaly and sensorineural deafness at NIH's Office of Rare Diseases
Arthrogryposis multiplex congenita CNS calcification at NIH's Office of Rare Diseases
Arthrogryposis multiplex congenita whistling face at NIH's Office of Rare Diseases
Arthrogryposis multiplex congenita at NIH's Office of Rare Diseases
Arthrogryposis ophthalmoplegia retinopathy at NIH's Office of Rare Diseases
Arthrogryposis renal dysfunction cholestasis syndrome at NIH's Office of Rare Diseases

ncbi.nlm.nih.gov

Kalampokas E, Kalampokas T, Sofoudis C, Deligeoroglou E, Botsis D (2012). "Diagnosing arthrogryposis multiplex congenita: a review". ISRN Obstetrics and Gynecology. 2012: 264918. doi:10.5402/2012/264918. PMC 3461621. PMID 23050160.
Bamshad M, Van Heest AE, Pleasure D (July 2009). "Arthrogryposis: a review and update". The Journal of Bone and Joint Surgery. American Volume. 91 (Suppl 4): 40–6. doi:10.2106/JBJS.I.00281. PMC 2698792. PMID 19571066.
Fassier A, Wicart P, Dubousset J, Seringe R (October 2009). "Arthrogryposis multiplex congenita. Long-term follow-up from birth until skeletal maturity". Journal of Children's Orthopaedics. 3 (5): 383–90. doi:10.1007/s11832-009-0187-4. PMC 2758174. PMID 19669823.
Schrander-Stumpel CT, Höweler CJ, Reekers AD, De Smet NM, Hall JG, Fryns JP (January 1993). "Arthrogryposis, ophthalmoplegia, and retinopathy: confirmation of a new type of arthrogryposis". Journal of Medical Genetics. 30 (1): 78–80. doi:10.1136/jmg.30.1.78. PMC 1016242. PMID 8423615.
Binkiewicz-Glinska A, Sobierajska-Rek A, Bakula S, Wierzba J, Drewek K, Kowalski IM, Zaborowska-Sapeta K (November 2013). "Arthrogryposis in infancy, multidisciplinary approach: case report". BMC Pediatrics. 13 (1): 184. doi:10.1186/1471-2431-13-184. PMC 3833971. PMID 24215600.
Matar HE, Beirne P, Garg N (February 2016). "The effectiveness of the Ponseti method for treating clubfoot associated with arthrogryposis: up to 8 years follow-up". Journal of Children's Orthopaedics. 10 (1): 15–8. doi:10.1007/s11832-016-0712-1. PMC 4763152. PMID 26833334.
El-Sobky TA, Samir S, Mahmoud S (July 2020). "Naviculectomy for two ambulatory children with intractable congenital vertical talus: redefining the indications of an old technique". Journal of Pediatric Orthopedics. Part B. 29 (4): 387–391. doi:10.1097/BPB.0000000000000663. PMC 7255489. PMID 31356503.

ghr.nlm.nih.gov

"Sheldon-Hall syndrome". Genetics Home Reference. Retrieved 2019-09-12.

omim.org

Online Mendelian Inheritance in Man (OMIM): 301830

orpha.net

"ORPHA1139 Arthrogryposis - epileptic seizures - migrational brain disorder". Orphanet.ORPHANET - About rare diseases - About orphan drugs
"ORPHANET - About rare diseases - About orphan drugs". Archived from the original on 2005-11-04. Retrieved 2007-04-25.
ORPHANET - About rare diseases - About orphan drugs Archived December 26, 2004, at the Wayback Machine
ORPHANET - About rare diseases - About orphan drugs
ORPHANET - About rare diseases - About orphan drugs
ORPHANET - About rare diseases - About orphan drugs

peacehealth.org

Gordon Syndrome Archived September 27, 2007, at the Wayback Machine

researchgate.net

Tiemann, Christian; Bührer, Christoph; Burwinkel, Barbara; Wirtenberger, Michael; Hoehn, Thomas; Hübner, Christoph; van Landeghem, Frank; Stoltenburg-Didinger, Gisela; Obladen, Michael (2005-08-30). "Arthrogryposis multiplex with deafness, inguinal hernias, and early death: A family report of a probably autosomal recessive trait". American Journal of Medical Genetics. Part A. 137 (2): 125–129. doi:10.1002/ajmg.a.30860. PMID 16059941. S2CID 41345689.

sciencedaily.com

"Researchers combat developmental delays with 'super suits'". Science Daily. May 17, 2016. Retrieved 10 May 2017.

sciencehistory.org

Maguire G (April 21, 2017). "Learning to Move with Move to Learn". Distillations Blog. Archived from the original on 23 March 2018. Retrieved 22 March 2018.

semanticscholar.org

api.semanticscholar.org

Miller M, Dobbs MB (October 2015). "Congenital Vertical Talus: Etiology and Management". The Journal of the American Academy of Orthopaedic Surgeons. 23 (10): 604–11. doi:10.5435/JAAOS-D-14-00034. PMID 26337950. S2CID 2282828.
Rink BD (June 2011). "Arthrogryposis: a review and approach to prenatal diagnosis". Obstetrical & Gynecological Survey. 66 (6): 369–77. doi:10.1097/OGX.0b013e31822bf5bb. PMID 21851751. S2CID 34468857.
Smit LM, Barth PG (June 1980). "Arthrogryposis multiplex congenita due to congenital myasthenia". Developmental Medicine and Child Neurology. 22 (3): 371–4. doi:10.1111/j.1469-8749.1980.tb03718.x. PMID 6446471. S2CID 39261871.
Illum N, Reske-Nielsen E, Skovby F, Askjaer SA, Bernsen A (November 1988). "Lethal autosomal recessive arthrogryposis multiplex congenita with whistling face and calcifications of the nervous system". Neuropediatrics. 19 (4): 186–92. doi:10.1055/s-2008-1052443. PMID 3205375. S2CID 260242391.
Tiemann, Christian; Bührer, Christoph; Burwinkel, Barbara; Wirtenberger, Michael; Hoehn, Thomas; Hübner, Christoph; van Landeghem, Frank; Stoltenburg-Didinger, Gisela; Obladen, Michael (2005-08-30). "Arthrogryposis multiplex with deafness, inguinal hernias, and early death: A family report of a probably autosomal recessive trait". American Journal of Medical Genetics. Part A. 137 (2): 125–129. doi:10.1002/ajmg.a.30860. PMID 16059941. S2CID 41345689.
Di Rocco M, Callea F, Pollice B, Faraci M, Campiani F, Borrone C (October 1995). "Arthrogryposis, renal dysfunction and cholestasis syndrome: report of five patients from three Italian families". European Journal of Pediatrics. 154 (10): 835–9. doi:10.1007/BF01959793. PMID 8529684. S2CID 32845371.

thefreedictionary.com

"The Free Dictionary: Arthrogryposis". Retrieved 11 July 2013.

acronyms.thefreedictionary.com

Arthrogryposis Multiplex Congenita, Neurogenic Type - What does AMCN stand for? Acronyms and abbreviations by the Free Online Dictionary

web.archive.org

"ORPHANET - About rare diseases - About orphan drugs". Archived from the original on 2005-11-04. Retrieved 2007-04-25.
ORPHANET - About rare diseases - About orphan drugs Archived December 26, 2004, at the Wayback Machine
Gordon Syndrome Archived September 27, 2007, at the Wayback Machine
"Arthrogryposis multiplex congenita distal type II associated with facial abnormality". Archived from the original on 2007-09-27. Retrieved 2007-04-25.
Chen E (27 January 2016). "Building functional, fashionable exoskeletons for babies". NewsWorks The Pulse. Archived from the original on 4 August 2017. Retrieved 10 May 2017.
Maguire G (April 21, 2017). "Learning to Move with Move to Learn". Distillations Blog. Archived from the original on 23 March 2018. Retrieved 22 March 2018.