Modified French Osteotomy for Humeroradial Synostosis in a Child with Multiple Synostoses Syndrome: A Case Report
نویسندگان
چکیده
منابع مشابه
Congenital humeroradial synostosis: a case report.
ABSTRACT We present here a unique case of humeroradial synostosis. These anomalies are due to longitudinal failure of differentiation. Approximately 150 cases of humeroradial synostosis have been reported worldwide, the majority of which are familial in nature or associated with syndromes. The case presented here involves an infant aged 1½ months, born with bilateral humeroradial synostosis wit...
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Non-syndromic bilateral humeroradial synostosis is a very rare congenital anomalies of the upper limbs. This condition often occurs in conjunction with various syndromes and is associated with a positive family history. Herein, we report a 6 year old boy with non-syndromic bilateral humeroradial synostosis, without aplasia, hypoplasia or family history. Both elbows were constant at 90 degrees f...
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Background Stevens-Johnson syndrome (SJS) is one of potentially fatal disorders that often occur after taking certain types of medication. There are reports of this disease after some infections. This paper presents the case of a young boy with idiopathic Stevens-Johnson syndrome. Case Report A six-year-old male patient with complaint of fever and skin lesions was transferred to emergency depar...
متن کاملFemoral-tibial-synostosis in a child with Roberts syndrome (Pseudothalidomide): a case report
BACKGROUND Roberts syndrome (Pseudothalidomide) is a rare birth defect that causes severe bone malformation complex. The bones of the arms, and in some cases other appendages, may be extremely shortened and even absent. The fingers of the hands may be fused. An extreme case results in the absence of the upper bones of both the arms and legs so that the hands and feet appear attached directly to...
متن کاملevidence for a new ad syndrome: report of a large iranian sibship with severe multiple synostosis
an investigation was carried out on a young unrelated couple, both 29 years old, with two boys and three girls, 3 months to 8 years old. one boy and the mother were healthy, the other four children and the father were affected. the family, originally from the district of nour, in northern iran, near the caspian sea, was first counseled at the genetic clinic in tehran in 1984. several trips were...
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ژورنال
عنوان ژورنال: Malaysian Orthopaedic Journal
سال: 2019
ISSN: 1985-2533,2232-111X
DOI: 10.5704/moj.1907.011