ArticleBMC pediatrics2007
A case of Cornelia de Lange syndrome from Sudan.
Article in BMC pediatrics, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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Who cites it
4 citing papers in PubMed, 10 citations in OpenAlex.
- Trajectories of child undernutrition in Ethiopia: a multivariate GEE approach.BMJ global health · 2026Article
- A Case Report of Cornelia De Lange Syndrome in Northern Iran; A Clinical and Diagnostic Study.Journal of clinical and diagnostic research : JCDR · 2016Article
- Cornelia de Lange syndrome - characteristics and laparoscopic treatment modalities of reflux based on own material.Wideochirurgia i inne techniki maloinwazyjne = Videosurgery and other miniinvasive techniques · 2011Article
- Cornelia de lange syndrome.Indian journal of human genetics · 2008Article
Corrections and comments
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Authors and funding
6 authors at 3 institutions in 2 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundBrachmann de Lange syndrome (BDLS) is a multiple congenital anomaly syndrome characterized by a distinctive facial appearance, prenatal and postnatal growth deficiency, psychomotor delay, behavioral problems, and malformations of the upper extremities. CASE PRESENTATION: Here we present for the first time a case of BDLS from Sudan, a 7-month-old female infant, who was referred as a case of malnutrition. The patient was from a Sudanese western tribe. Clinical investigation showed that the child was a classical case of BDLS, but with some additional clinical findings not previously reported including crowded ribs and tied tongue.
conclusionReporting BDLS cases of different ethnic backgrounds could add nuances to the phenotypic description of the syndrome and be helpful in diagnosis.
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