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Journal articles on the topic 'Ectrodactylie'

Author: Grafiati

Published: 4 June 2021

Last updated: 4 February 2022

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1

Pinette, Michael, Louis Garcia, Joseph R. Wax, Angelina Cartin, and Jacquelyn Blackstone. "Familial Ectrodactyly." Journal of Ultrasound in Medicine 25, no. 11 (November 2006): 1465–67. http://dx.doi.org/10.7863/jum.2006.25.11.1465.

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2

Bharati, Anamika, Saumya Navit, Suleman Abbas Khan, Seema Jabeen, Nishi Grover, and Meenakshi Upadhyay. "Ectrodactyly-Ectodermal Dysplasia Clefting Syndrome: A Case Report of Its Dental Management with 2 Years Follow-Up." Case Reports in Dentistry 2020 (March 23, 2020): 1–5. http://dx.doi.org/10.1155/2020/8418725.

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Ectrodactyly-ectodermal dysplasia clefting syndrome is a rare genetic disorder characterized by the triad of ectrodactyly-ectodermal dysplasia and facial clefting of lip or palate or both along with some systemic manifestations. Although each defect that comprises the syndrome has been known to occur as a separate entity, the congregation of all three anomalies in a single individual appears to be an extremely rare occurrence, with incidence being approximately 1.5/100 million population. Early diagnosis and management of clinical manifestations associated with ectrodactyly-ectodermal dysplasia clefting syndrome present a unique challenge. We report a case of this rare disorder in an 11-year-old male patient along with its dental management using a multidisciplinary approach.

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3

Rivera, Horacio. "Ectrodactyly and 7q22.1." American Journal of Medical Genetics 53, no. 1 (October 15, 1994): 89. http://dx.doi.org/10.1002/ajmg.1320530121.

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4

Lévy, Jonathan, Jean-Marie Jouannic, Julien Saada, Ferdinand Dhombres, Jean-Pierre Siffroi, and Marie-France Portnoï. "Prenatal Diagnosis of Bilateral Ectrodactyly and Radial Agenesis Associated with Trisomy 10 Mosaicism." Case Reports in Genetics 2013 (2013): 1–4. http://dx.doi.org/10.1155/2013/592702.

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Ectrodactyly or split hand and foot malformations (SHFMs) are rare malformations of the limbs, characterized by median clefts of the hands and feet, syndactyly, and aplasia and/or hypoplasia of the phalanges. They represent a clinically and genetically heterogeneous disorder, with both sporadic and familial cases. Most of the genomic rearrangements identified to date in some forms of SHFM are autosomal dominant traits, involving various chromosome regions. Bilateral radial ray defects comprise also a large heterogenous group of disorders, including trisomy 18, Fanconi anemia, and thrombocytopenia-absent-radius syndrome, not commonly associated with ectrodactyly. The present paper describes a case of ectrodactyly associated with bilateral radial ray defects, diagnosed in the first trimester of pregnancy, in a fetus affected by trisomy 10. Only four cases of sporadic and isolated ectrodactyly, diagnosed by ultrasonography between 14 and 22 weeks’ gestation, have been reported. To our knowledge, the present case is the first report of mosaic trisomy 10 associated with SHFM and radial aplasia. Trisomy 10 is a rare lethal chromosomal abnormality, most frequently found in abortion products. Only six liveborn mosaic trisomy 10 infants, with severe malformations, dead in early infancy, have been reported. A severe clinical syndrome can be defined, comprising ear abnormalities, cleft lip/palate, malformations of eyes, heart, and kidneys, and deformity of hands and feet and most often associated with death neonatally or in early infancy.

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5

Keyal, K., BG Joshi, R. Pandey, and BM Shrestha. "Ectrodactyly: A rare anomaly of limbs." Journal of Nepal Paediatric Society 31, no. 3 (September 19, 2011): 235–37. http://dx.doi.org/10.3126/jnps.v31i3.4429.

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Split-hand/split-foot malformation (SHFM) is a rare congenital malformation of the limbs with median clefts of the hands and feet and aplasia/hypoplasia of the phalanges, metacarpals and metatarsals. When present as an isolated anomaly, it is usually inherited as an autosomal dominant form. We report a case of nonsyndromic form of ectrodactyly because of its rarity. Key words: Split-hand/split-foot malformation; Nonsyndromic ectrodactyly DOI: http://dx.doi.org/10.3126/jnps.v31i3.4429 J Nep Paedtr Soc 2011;31(3): 235-237

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6

Mandal, Subhra, Prabir Mandal, and Panchanan Kundu. "MEDICAL MYSTERY: ECTRODACTYLY A CASE REPORT." International Journal of Anatomy and Research 3, no. 1 (January 31, 2015): 845–47. http://dx.doi.org/10.16965/ijar.2015.101.

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7

Mondal, Monojit, Kriti Sundar Rana, Nayan Banerji, Sayan Bose, Tanmoy Biswas, Biswajit Biswas, and Pijush Kanti Mandal. "Split-hand/split-foot malformation (SHFM)." Asian Journal of Medical Sciences 6, no. 1 (July 26, 2014): 122–23. http://dx.doi.org/10.3126/ajms.v6i1.10018.

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Split-hand/split-foot malformation (SHFM), also known as ectrodactyly or lobster claw hand is a congenital limb malformation, characterized by a deep median cleft of the hand and/or foot due to the absence of the central rays of the autopod. It may occur singly or in association with syndromes, former being mostly autosomal dominant but autosomal recessive variety is rare. We are reporting a case of ectrodactyly with autosomal recessive mode of inheritance DOI: http://dx.doi.org/10.3126/ajms.v6i1.10018 Asian Journal of Medical Sciences Vol.6(1) 2015 122-123

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8

YOUNG, I. D., J. M. ZUCCOLLO, M. BARROW, and A. FOWLIE. "Holoprosencephaly, telecanthus and ectrodactyly." Clinical Dysmorphology 1, no. 1 (January 1992): 47???52. http://dx.doi.org/10.1097/00019605-199201000-00008.

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9

TURNPENNY, P. D., A. W. JOHNSTON, J. C. S. DEAN, N. E. HAITES, D. A. COUZIN, and G. S. STEPHEN. "Ectrodactyly-mandibulo-facial dysostosis." Clinical Dysmorphology 1, no. 2 (April 1992): 103???110. http://dx.doi.org/10.1097/00019605-199204000-00006.

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10

LANDY, S. J., and D. DONNAI. "A new ectrodactyly syndrome?" Clinical Dysmorphology 2, no. 2 (April 1993): 169???172. http://dx.doi.org/10.1097/00019605-199304000-00014.

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11

Evans, Jane A., Martin H. Reed, and Cheryl R. Greenberg. "Fibular aplasia with ectrodactyly." American Journal of Medical Genetics 113, no. 1 (November 15, 2002): 52–58. http://dx.doi.org/10.1002/ajmg.10754.

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12

Nair, S. B., G. Mukundan, R. Thomas, and K. K. Gopinathan. "Ectrodactyly and Prenatal Diagnosis." Journal of Obstetrics and Gynecology of India 61, no. 6 (December 2011): 683–85. http://dx.doi.org/10.1007/s13224-012-0120-5.

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13

Qureshi, Ihtesham A., Rohit Kumar Gudepu, Ravikanth Chava, Sravya Emmani, Syed Husain Asghar, Mohtashim A. Qureshi, and Nimmathota Arlappa. "Case Report: Gollop-Wolfgang Complex in a 5 month old baby." F1000Research 3 (February 9, 2015): 315. http://dx.doi.org/10.12688/f1000research.5889.2.

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Skeletal dysplasias are disorders associated with a generalized abnormality in the skeleton. The Gollop-Wolfgang complex (GWC) is a limb deficiency disorder and an unusual limb malformation with highly variable manifestations. Here we report an interesting case of a 5-month old male baby from India with Gollop-Wolfgang Complex showing bifurcation of the right femur, ectrodactyly of both feet, ectrodactyly of left hand, syndactyly of right hand and unusual presentation of bilateral fibular agenesis and caudal (Sacrococcygeal) agenesis. The etiology of GWC in this 5 month old male baby could possibly be attributed to spontaneous gene mutation. The clinical, radiographic findings and the unusual presentation are presented in detail

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14

Qureshi, Ihtesham A., Rohit Kumar Gudepu, Ravikanth Chava, Sravya Emmani, Syed Husain Asghar, Mohtashim A. Qureshi, and Nimmathota Arlappa. "Case Report: Gollop-Wolfgang Complex in a 5 month old baby." F1000Research 3 (February 24, 2015): 315. http://dx.doi.org/10.12688/f1000research.5889.3.

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Skeletal dysplasias are disorders associated with a generalized abnormality in the skeleton. The Gollop-Wolfgang complex (GWC) is a limb deficiency disorder and an unusual limb malformation with highly variable manifestations. Here we report an interesting case of a 5-month old male baby from India with Gollop-Wolfgang Complex showing bifurcation of the right femur, ectrodactyly of both feet, ectrodactyly of left hand, syndactyly of right hand and unusual presentation of bilateral fibular agenesis and caudal (Sacrococcygeal) agenesis. The etiology of GWC in this 5 month old male baby could possibly be attributed to spontaneous gene mutation. The clinical, radiographic findings and the unusual presentation are presented in detail.

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15

Akahori, Yoichiro, Hisashi Masuyama, Yumi Masumoto, and Yuji Hiramatsu. "Three-Dimensional Ultrasound Findings in Cornelia de Lange Syndrome: A Case Report." Case Reports in Obstetrics and Gynecology 2012 (2012): 1–4. http://dx.doi.org/10.1155/2012/568351.

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Introduction. The objective is to report a case of Cornelia de Lange syndrome (CdLS) diagnosed by detailed observations using three-dimensional sonography.Case Report. A 33-year-old healthy multipara was referred to our hospital at 34-week gestation after severe fetal growth restriction, congenital heart anomaly, and antebrachium abnormality were diagnosed during the third trimester. Further sonography diagnosis on cardiac abnormalities diagnosed the existence of ventricular septal defect in the outflow tract, atrioventricularis communis, and truncus arteriosus communis where the pulmonary artery branched from the common arterial trunk. As for abnormalities of the forearms, ectrodactylia and monodactylism were suspected and the abnormalities were observed sterically by using three-dimensional sonography. A 1986 g (1.07 percentile) male newborn was delivered by assisted breech extraction at 37-week gestation. After birth, from characteristic facies including bushy eyebrow, broad nasal bridge, micrognathia, and abnormalities of the forearms (ectrodactylia and monodactylism), the case was diagnosed with CdLS.Conclusion. Through detailed observation including abnormalities of fingers, we could exemplify this very rare disease as an antenatal diagnoses for fetal growth retardation.

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16

Qureshi, Ihtesham A., Rohit Kumar Gudepu, Ravikanth Chava, Sravya Emmani, Syed Husain Asghar, Mohtashim A. Qureshi, and Nimmathota Arlappa. "Case Report: Gollop-Wolfgang Complex in a 5 month old baby." F1000Research 3 (December 23, 2014): 315. http://dx.doi.org/10.12688/f1000research.5889.1.

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Abstract:

Skeletal dysplasias are disorders associated with a generalized abnormality in the skeleton. The Gollop-Wolfgang complex (GWC) is a limb deficiency disorder and an unusual limb malformation with highly variable manifestations. Here we report the interesting case of a 5-month old male baby from India with Gollop-Wolfgang Complex showing bifurcation of the right femur, ectrodactyly of both feet, ectrodactyly of left hand, syndactyly of right hand and unusual presentation of bilateral fibular agenesis and caudal (Sacrococcygeal) agenesis. The etiology of GWC in this 5 month old male baby could possibly be attributed to spontaneous gene mutation due to consanguineous marriage of his parents. The clinical, radiographic findings and the unusual presentation are presented in detail.

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17

Mônico, Alexander Tamanini, Thiago Silva-Soares, and Esteban Diego Koch. "Malformation in three anuran species from a preserved remnant of Atlantic Forest in southeastern Brazil." Neotropical Biology and Conservation 14, no. 2 (July 22, 2019): 213–20. http://dx.doi.org/10.3897/neotropical.14.e37919.

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Records of malformation in amphibians have significantly increased on a global scale. The main causes of malformations are linked to environmental contaminants, and records in preserved environments are uncommon. We reported malformations in three anuran species belonging to three families: Crossodactylustimbuhy (Hylodidae), Proceratophrysschirchi (Odontophrynidae) and Thoropamiliaris (Cycloramphidae). All records were found within the Reserva Biológica Augusto Ruschi, a well-preserved protected remnant of Atlantic rainforest located in the mountains of the state of Espírito Santo, southeastern Brazil. The malformations detected were hemimelia (long bone shortened) with ectrodactyly (digit absent) and brachydactyly (digit shortened) in C.timbuhy, microphtalmia (small eye) in P.schirchi and ectrodactyly in T.miliaris. Further studies are recommended to enable a better understanding about the incidence and causes of malformations within preserved areas.

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18

Moorthy, Dr N. L. N. "Aplasia of Tibia –Ectrodactyly Syndrome – A Rare Disease." Journal of Medical Science And clinical Research 05, no. 06 (June 26, 2017): 23919–21. http://dx.doi.org/10.18535/jmscr/v5i6.187.

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19

Aneesha, Dr Dama, Dr Geetha Lakshmi, and Dr K. Saraswathi. "Ectrodactyly or Lobster Claw Syndrome,." IOSR Journal of Dental and Medical Sciences 16, no. 07 (July 2017): 46–49. http://dx.doi.org/10.9790/0853-1607024649.

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20

Libbie, JC, FF Derk, and AJ Nardozza. "Ectrodactyly. A unique case presentation." Journal of the American Podiatric Medical Association 86, no. 8 (August 1, 1996): 398–400. http://dx.doi.org/10.7547/87507315-86-8-398.

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21

Kelman, GJ, and RC Aronoff. "Ectrodactyly-ectodermal dysplasia-clefting syndrome." Journal of the American Podiatric Medical Association 90, no. 9 (October 1, 2000): 460–64. http://dx.doi.org/10.7547/87507315-90-9-460.

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Ectrodactyly-ectodermal dysplasia-clefting syndrome is a rare congenital anomaly that affects tissues of mesodermal and ectodermal origin. Musculoskeletal involvement frequently requires orthopedic intervention. The authors present a review of the literature pertaining to this rare syndrome as well as a case report of a female patient who exhibited the complete clinical triad. A description of the surgical management of her condition is also presented.

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22

Jindal, Geetanjali, VeenaR Parmar, and VipulGupta Kumar. "Ectrodactyly/split hand feet malformation." Indian Journal of Human Genetics 15, no. 3 (2009): 140. http://dx.doi.org/10.4103/0971-6866.60191.

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23

Adanali, Gokhan, Dilek ??enen, Meltem Ayhan, and B??lent Erdogan. "Ectrodactyly???Ectodermal Dysplasia Clefting Syndrome." Annals of Plastic Surgery 47, no. 3 (September 2001): 350. http://dx.doi.org/10.1097/00000637-200109000-00028.

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24

Turnpenny, Peter D. "Ectrodactyly with multiple congenital abnormalities." American Journal of Medical Genetics 44, no. 2 (September 15, 1992): 253. http://dx.doi.org/10.1002/ajmg.1320440233.

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25

Fried, K. "Ectrodactyly, cleft lip/palate syndrome." American Journal of Medical Genetics 44, no. 3 (October 1, 1992): 387. http://dx.doi.org/10.1002/ajmg.1320440326.

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26

Urioste, Miguel, María Luisa Martínez-Frías, and Paulino Aparicio. "Ectrodactyly in trisomy 13 syndrome." American Journal of Medical Genetics 53, no. 4 (December 1, 1994): 390–92. http://dx.doi.org/10.1002/ajmg.1320530422.

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27

Rodini, Elaine S. O., J. A. S. Freitas, and A. Richieri-Costa. "Ectrodactyly, cleft lip/palate syndrome." American Journal of Medical Genetics 38, no. 4 (March 15, 1991): 539–41. http://dx.doi.org/10.1002/ajmg.1320380408.

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28

Di Pietro, Simona, Giuseppe Santi Rapisarda, Luca Cicero, Vito Angileri, Simona Morabito, Giovanni Cassata, and Francesco Macrì. "Four Unusual Cases of Congenital Forelimb Malformations in Dogs." Animals 11, no. 3 (March 14, 2021): 813. http://dx.doi.org/10.3390/ani11030813.

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Four dogs were presented with thoracic limb deformity. After clinical and radiographic examinations, a diagnosis of congenital malformations was performed for each of them. In one case, a deformity involving both the radial and ulnar side of the distal limb was observed. Based on clinical and radiological evaluations, a diagnosis of postaxial terminal longitudinal ulnar hemimelia was performed. The term ectrodactyly was used to refer different malformations characterized by skin and soft tissue separation of the distal forelimb observed in two dogs. Simple complete uncomplicated syndactyly of the right forelimb, and complex incomplete uncomplicated syndactyly of the left forelimb were diagnosed in the fourth case. To the authors’ knowledge, ectrodactyly and simple complete uncomplicated syndactyly are very uncommon anomalies in companion animals and have been rarely documented. Moreover, postaxial terminal longitudinal ulnar hemimelia has still not been reported in dogs.

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29

Ferreira, Márcio Poletto, Marcelo Meller Alievi, Isis Dos Santos Dal-Bó, Fernanda Silveira Nóbrega, Paula Cristina Sieczkowski Gonzalez, and Carlos Afonso de Castro Beck. "Surgical management of ectrodactyly in a dog." Semina: Ciências Agrárias 37, no. 2 (April 26, 2016): 891. http://dx.doi.org/10.5433/1679-0359.2016v37n2p891.

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Ectrodactyly is the term used to designate cases in which soft and bone tissue separation within the distal region of the thoracic limbs is present. It is observed in particular below the metacarpal bones and extending to the radius and ulna. In addition, it can often be associated with ipsilateral elbow luxation. We describe a case of ectrodactyly in a 3-month-old mongrel dog, where bone and soft tissue separation occurred between the third and fourth digits, extending proximally to the carpal region. We identified shortening of the ulna without elbow luxation. The dog was subjected to a surgical procedure comprising bone and soft tissue reconstruction and ulnar diaphyseal osteotomy, which was fixed using a Steinmann pin in the intramedullary canal, maintaining a distance of 1 cm between the two ulnar fragments. Two distal phalanges were removed because it was not possible to reposition them anatomically in the limb. The dog walked with mild lameness nine months after surgery.

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30

Massafra, C., M. Bartolozzi, P. Bartolozzi, and L. Scillone. "Rokitansky-Küster-Hauser syndrome with ectrodactyly." Acta Obstetricia et Gynecologica Scandinavica 67, no. 6 (January 1988): 557–60. http://dx.doi.org/10.3109/00016348809029870.

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31

Najmuddin, Mohammed, SafeenaAbdul Khader Saheb, Tenny John, and Sameena Parveen. "Ectrodactyly and oligodontia a rare association." West African Journal of Radiology 23, no. 2 (2016): 130. http://dx.doi.org/10.4103/1115-1474.164867.

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32

Ortonne, Jean-Paul, Llnnart Juhlin, and Jean-Philippe Lacour. "Anonychia with Ectrodactyly of One Foot." International Journal of Dermatology 25, no. 3 (April 1986): 188. http://dx.doi.org/10.1111/j.1365-4362.1986.tb02216.x.

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33

Mufti, M. H., and S. K. Wood. "Ectrodactyly in sisters and half sisters." Journal of Medical Genetics 24, no. 4 (April 1, 1987): 220–24. http://dx.doi.org/10.1136/jmg.24.4.220.

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34

Hennekam, R. C., and E. J. Lommen. "Ectrodactyly in sisters and half sisters." Journal of Medical Genetics 25, no. 2 (February 1, 1988): 134–35. http://dx.doi.org/10.1136/jmg.25.2.134.

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35

SVSG, Nirmala, Sandeep Chilamakuri, Chaitanya Pavuluri, Sivakumar Nuvvula, and Sindhuri Veluru. "Ectrodactyly: A rare anomaly of limbs." Journal of Dr. NTR University of Health Sciences 4, no. 1 (2015): 53. http://dx.doi.org/10.4103/2277-8632.153329.

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36

Mishra, Parag, Mamta Muranjan, and B. A. Bharucha. "Autosomal dominant ectrodactyly with sensorineural deafness." Clinical Dysmorphology 9, no. 2 (April 2000): 119–21. http://dx.doi.org/10.1097/00019605-200009020-00009.

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37

Silengo, M. Cirillo, M. Biagioli, G. Lopez Bell, G. Bona, and P. Franceschini. "Triphalangeal thumb and brachy-ectrodactyly syndrome." Clinical Genetics 31, no. 1 (June 28, 2008): 13–18. http://dx.doi.org/10.1111/j.1399-0004.1987.tb02761.x.

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38

Moshegov, Con N. "Ectrodactyly-Ectodermal Dysplasia-Clefting (EEC) Syndrome." Archives of Ophthalmology 114, no. 10 (October 1, 1996): 1290. http://dx.doi.org/10.1001/archopht.1996.01100140490032.

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39

Rogers, R. Curtis. "Trisomy 18 with unilateral atypical ectrodactyly." American Journal of Medical Genetics 49, no. 1 (January 1, 1994): 125–26. http://dx.doi.org/10.1002/ajmg.1320490125.

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40

Ray, Sanghamitra, and Prakash Chand Jain. "Nonsyndromic Split Hand/ Foot Malformation: Ectrodactyly." Journal of Nepal Paediatric Society 36, no. 1 (October 22, 2016): 103–4. http://dx.doi.org/10.3126/jnps.v36i1.14662.

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The CaseA three year old girl came to our OPD with deformity of left hand called ectrodactyly. She had no other deformities, dysmorphic features and was developmentally appropriate. The X-ray of the hand showed normal radius, ulna and metacarpals but absence of phalanges of the middle three fingers of left hand. She was examined in detail for any ectodermal anomaly, clefting of lip or palate. USG abdomen, kidney and urinary tract was done to rule out any urinary tract malformation. She was finally referred to higher centre for reconstructive surgery for ectrodactyly.J Nepal Paediatr Soc 2016;36(1):103-104

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41

JANCAR, J. "ECTRODACTYLY, SPASTIC PARAPLEGIA AND MENTAL RETARDATION." Journal of Intellectual Disability Research 11, no. 3 (June 28, 2008): 207–11. http://dx.doi.org/10.1111/j.1365-2788.1967.tb00221.x.

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42

Fried, K. "Ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome." Clinical Genetics 3, no. 5 (April 23, 2008): 396–400. http://dx.doi.org/10.1111/j.1399-0004.1972.tb01473.x.

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43

Salvi, Andrea Emilio, Angelo Chessa, and Massimo Pezzoni. "A Clinical Picture of Ectrodactyly Hand." JCR Journal of Clinical Rheumatology 21, no. 3 (April 2015): 165. http://dx.doi.org/10.1097/rhu.0000000000000240.

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44

Elmann, Solly, Sarah A. Hanson, Christopher N. Bunce, and Roman Shinder. "Ectrodactyly Ectodermal Dysplasia Clefting (EEC) Syndrome." Ophthalmic Plastic and Reconstructive Surgery 31, no. 2 (2015): e35-e37. http://dx.doi.org/10.1097/iop.0000000000000060.

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45

Gün, Ismet, Cem Kizilaslan, and Mehmet Aral Atalay. "Familial ectrodactyly-ectodermal dysplasia-clefting syndrome." International Journal of Gynecology & Obstetrics 119, no. 1 (July 12, 2012): 86–87. http://dx.doi.org/10.1016/j.ijgo.2012.05.014.

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46

Gamito-Gómez, Araceli, Rodrigo Gutierrez-Quintana, and Annette Wessmann. "Congenital Malformations Resembling VACTERL Association in a Golden Retriever." Journal of the American Animal Hospital Association 54, no. 1 (January 1, 2018): 60–64. http://dx.doi.org/10.5326/jaaha-ms-6236.

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ABSTRACT A 2 mo old golden retriever presented with malformation of the left thoracic limb and a small circular indentation of the skin in the cranial thoracic spine. Radiographs showed a cleft between the second and fifth metacarpal bones of the left thoracic limb compatible with ectrodactyly and spina bifida affecting T4 and T5 vertebrae. Magnetic resonance imaging of the thoracic spine showed dorsal reposition of the spinal cord and a tract connecting from the dura mater to the skin. No other malformations were detected. Surgical excision of the tract was performed and histopathological examination diagnosed a dermoid sinus type IV. Dermoid sinus and spina bifida are well-recognized congenital spinal and spinal cord defects, yet association with other congenital malformation are rarely reported in dogs. The here-reported dog had spinal and spinal cord abnormalities with concurrent limb malformation, which are two components of a nonrandom association of birth defects described as VACTERL in people. To the authors' knowledge, this is the first report describing concurrent dermoid sinus type IV, spina bifida, and ectrodactyly in a dog, and highlights the importance of patient examination for occurrence of multiple malformations to provide an appropriate prognosis for an owner.

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47

Seno, Hisakazu, Akira Yanai, Hiroko Sugino, Masahiro Inoue, Takako Takei, and Iyoko Miyake. "Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip Syndrome." Scandinavian Journal of Plastic and Reconstructive Surgery and Hand Surgery 30, no. 3 (January 1996): 227–30. http://dx.doi.org/10.3109/02844319609062820.

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48

Kalathia, MitulB, AvaniA Seta, and ParinN Parmar. "A case of ectrodactyly in a neonate." Journal of Clinical Neonatology 2, no. 3 (2013): 151. http://dx.doi.org/10.4103/2249-4847.120013.

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Obaid, Laila, Wafaa Al Rawi, Kamal Mustafa, and Ashraf Abuobayda. "Rare presentation of ectrodactyly in trisomy 13." Journal of Clinical Neonatology 9, no. 2 (2020): 143. http://dx.doi.org/10.4103/jcn.jcn_130_16.

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Grossi, Mariana, Luciane Pereira, Augusto Hinterholz, Mariana Nascimento, Daniela Miranda, and Fátima Souza. "Ectrodactyly: A rare malformation of the limbs." Residência Pediátrica 7, no. 1 (April 2017): 33–35. http://dx.doi.org/10.25060/residpediatr-2017.v7n1-07.

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