Literature DB >> 7726374

Experience of King Faisal Specialist Hospital and Research Center with Saudi organic acid disorders.

M Rashed1, P T Ozand, A al Aqeel, G G Gascon.   

Abstract

The Inborn Errors of Metabolism and Neurology Services of the King Faisal Specialist Hospital and Research Centre (KFSH&RC) and Armed Forces Hospital have received more than 1,500 patients suspected of having an organic acid disorder (OAD) during a period of four years. Of these, 307 patients suspected of having an organic acid disorder (OAD) during a period of four years. Of these, 307 patients, approximately 20%, had a clearly identifiable disorder. Identified OAD's constituted one-quarter of all patients diagnosed as having various types of inborn errors of metabolism during this period, in these clinical services. Prolonged follow-up was available in the majority of cases, allowing detailed clinical, neuroradiologic and neurophysiologic descriptions. Fifty patients (16%) had rare disorders by standards in the West. Approximately 25% were 'neurologic organic acidurias.' This is a new term we are introducing for OAD's manifesting primarily with neurologic signs, but without appreciable acidosis, hypoglycemia or hyperammonemia. In this special issue, we present the KFSH&RC experience with the rare disorders as individual articles. We estimate the frequency of OAD's in Saudi Arabia as 1/740 births. The increased frequency of OAD's in Saudi Arabia is probably due to increased consanguinity, since most OAD's occurred in excess in certain tribes; and due to increased surveillance and testing by our group. Saudi Arabia provides a unique opportunity for research in this area of pediatrics.

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Year:  1994        PMID: 7726374     DOI: 10.1016/0387-7604(94)90090-6

Source DB:  PubMed          Journal:  Brain Dev        ISSN: 0387-7604            Impact factor:   1.961


  10 in total

1.  Selective screening for inborn errors of metabolism: the primary care-based model in rural Crete.

Authors:  A Evangeliou; C Lionis; H Michailidou; M Spilioti; A Kanitsakis; P Nikitakis; N Drakonakis; C Giannakopoulou; S Sbyrakis; A C Sewell; H J Boehles; J Smeitink; R A Wevers
Journal:  J Inherit Metab Dis       Date:  2001-12       Impact factor: 4.982

2.  Newborn screening: experiences in the Middle East and North Africa.

Authors:  A A Saadallah; M S Rashed
Journal:  J Inherit Metab Dis       Date:  2007-08-15       Impact factor: 4.982

3.  Diagnosis of major organic acidurias in children: two years experience at a tertiary care centre.

Authors:  M P Narayanan; Vaidyanathan Kannan; K P Vinayan; D M Vasudevan
Journal:  Indian J Clin Biochem       Date:  2011-02-01

4.  Incidence and Geographic Distribution of Succinic Semialdehyde Dehydrogenase (SSADH) Deficiency.

Authors:  Savita Verma Attri; Pratibha Singhi; Natrujee Wiwattanadittakul; Jyotindra N Goswami; Naveen Sankhyan; Gajja S Salomons; Jean-Baptiste Roullett; Ryan Hodgeman; Mahsa Parviz; K Michael Gibson; Phillip L Pearl
Journal:  JIMD Rep       Date:  2016-11-05

5.  Incidence and patterns of inborn errors of metabolism in the Eastern Province of Saudi Arabia, 1983-2008.

Authors:  Hissa Moammar; George Cheriyan; Revi Mathew; Nouriya Al-Sannaa
Journal:  Ann Saudi Med       Date:  2010 Jul-Aug       Impact factor: 1.526

Review 6.  Evolution in health and medicine Sackler colloquium: Consanguinity, human evolution, and complex diseases.

Authors:  A H Bittles; M L Black
Journal:  Proc Natl Acad Sci U S A       Date:  2009-09-23       Impact factor: 11.205

7.  A novel PCCB mutation in a Thai patient with propionic acidemia identified by exome sequencing.

Authors:  Thantrira Porntaveetus; Chalurmpon Srichomthong; Kanya Suphapeetiporn; Vorasuk Shotelersuk
Journal:  Hum Genome Var       Date:  2015-09-17

8.  Spectrum of mutations underlying Propionic acidemia and further insight into a genotype-phenotype correlation for the common mutation in Saudi Arabia.

Authors:  Mohamed H Al-Hamed; Faiqa Imtiaz; Zuhair Al-Hassnan; Mohammed Al-Owain; Hamad Al-Zaidan; Mohamed S Alamoudi; Eissa Faqeih; Majid Alfadhel; Ali Al-Asmari; M M Saleh; Fuad Almutairi; Nabil Moghrabi; Moeenaldeen AlSayed
Journal:  Mol Genet Metab Rep       Date:  2019-01-09

9.  Screening for organic acidurias and aminoacidopathies in high-risk Brazilian patients: Eleven-year experience of a reference center.

Authors:  Moacir Wajner; Angela Sitta; Aline Kayser; Marion Deon; Ana C Groehs; Daniella M Coelho; Carmen R Vargas
Journal:  Genet Mol Biol       Date:  2019-04-11       Impact factor: 1.771

10.  Diagnosis and clinical features of organic acidemias: A hospital-based study in a single center in Damascus, Syria.

Authors:  Hala Khalil Shennar; Diana Al-Asmar; Ahmad Kaddoura; Sahar Al-Fahoum
Journal:  Qatar Med J       Date:  2015-07-04
  10 in total

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