Literature DB >> 11470934

Mitochondrial cytopathy presenting with focal segmental glomerulosclerosis, hypoparathyroidism, sensorineural deafness, and progressive neurological disease.

R Hameed1, F Raafat, P Ramani, G Gray, H P Roper, D V Milford.   

Abstract

A 6 year old boy who presented with steroid unresponsive nephrotic syndrome is reported. He was found to have focal segmental glomerulosclerosis and associated hypoparathyroidism and sensorineural deafness. The child progressed to end stage renal failure and was successfully managed by dialysis and cadaveric renal transplantation. He later developed progressive neurological deterioration and mitochondrial myopathy and neuropathy was diagnosed.

Entities:  

Mesh:

Year:  2001        PMID: 11470934      PMCID: PMC1742114          DOI: 10.1136/pmj.77.910.523

Source DB:  PubMed          Journal:  Postgrad Med J        ISSN: 0032-5473            Impact factor:   2.401


  7 in total

1.  Brief report: autosomal dominant familial hypoparathyroidism, sensorineural deafness, and renal dysplasia.

Authors:  R W Bilous; G Murty; D B Parkinson; R V Thakker; M G Coulthard; J Burn; D Mathias; P Kendall-Taylor
Journal:  N Engl J Med       Date:  1992-10-08       Impact factor: 91.245

2.  Familial nephrosis, nerve deafness, and hypoparathyroidism.

Authors:  A Y Barakat; J B D'Albora; M M Martin; P A Jose
Journal:  J Pediatr       Date:  1977-07       Impact factor: 4.406

Review 3.  HDR syndrome (hypoparathyroidism, sensorineural deafness, renal dysplasia) associated with del(10)(p13).

Authors:  T Hasegawa; Y Hasegawa; T Aso; S Koto; T Nagai; Y Tsuchiya; K C Kim; H Ohashi; K Wakui; Y Fukushima
Journal:  Am J Med Genet       Date:  1997-12-31

4.  Bilateral sensorineural hearing loss associated with the point mutation in mitochondrial genome.

Authors:  T Oshima; N Ueda; K Ikeda; K Abe; T Takasaka
Journal:  Laryngoscope       Date:  1996-01       Impact factor: 3.325

5.  Autosomal recessive hypoparathyroidism with renal insufficiency and developmental delay.

Authors:  N J Shaw; D Haigh; G T Lealmann; G Karbani; J T Brocklebank; M J Dillon
Journal:  Arch Dis Child       Date:  1991-10       Impact factor: 3.791

6.  Successful cochlear implantation in a patient with MELAS syndrome.

Authors:  E L Rosenthal; P R Kileny; A Boerst; S A Telian
Journal:  Am J Otol       Date:  1999-03

7.  A case of mitochondrial cytopathy with a typical point mutation for MELAS, presenting with severe focal-segmental glomerulosclerosis as main clinical manifestation.

Authors:  F Kurogouchi; T Oguchi; E Mawatari; S Yamaura; K Hora; M Takei; Y Sekijima; S i Ikeda; K Kiyosawa
Journal:  Am J Nephrol       Date:  1998       Impact factor: 3.754

  7 in total
  8 in total

1.  Muscular dystonia and athetosis in six patients with congenital nephrotic syndrome of the Finnish type (NPHS1).

Authors:  Hanne Laakkonen; Tuula Lönnqvist; Johanna Uusimaa; Erik Qvist; Leena Valanne; Matti Nuutinen; Marja Ala-Houhala; Kari Majamaa; Hannu Jalanko; Christer Holmberg
Journal:  Pediatr Nephrol       Date:  2005-12-17       Impact factor: 3.714

2.  Automated peritoneal dialysis for a patient with hearing loss: a case report.

Authors:  Tsutomu Sakurada; Shigeki Kojima; Daisuke Oishi; Kenichiro Koitabashi; Yugo Shibagaki; Kenjiro Kimura
Journal:  Perit Dial Int       Date:  2015 Mar-Apr       Impact factor: 1.756

3.  Respiratory chain deficiency presenting as congenital nephrotic syndrome.

Authors:  Alice Goldenberg; Linh Huynh Ngoc; Marie-Christine Thouret; Valérie Cormier-Daire; Marie-France Gagnadoux; Dominique Chrétien; Catherine Lefrançois; Vanna Geromel; Agnès Rötig; Pierre Rustin; Arnold Munnich; Véronique Paquis; Corinne Antignac; Marie-Claire Gubler; Patrick Niaudet; Pascale de Lonlay; Etienne Bérard
Journal:  Pediatr Nephrol       Date:  2005-01-29       Impact factor: 3.714

4.  Renal pathology in children with mitochondrial diseases.

Authors:  Elena Martín-Hernández; M Teresa García-Silva; Julia Vara; Yolanda Campos; Ana Cabello; Rafael Muley; Pilar Del Hoyo; Miguel Angel Martín; Joaquín Arenas
Journal:  Pediatr Nephrol       Date:  2005-06-24       Impact factor: 3.714

5.  Respiratory-chain deficiency presenting as diffuse mesangial sclerosis with NPHS3 mutation.

Authors:  Esra Baskin; Umut Selda Bayrakci; Füsun Alehan; Handan Ozdemir; Ayse Oner; Rita Horvath; Virginia Vega-Warner; Friedhelm Hildebrandt; Fatih Ozaltin
Journal:  Pediatr Nephrol       Date:  2011-03-02       Impact factor: 3.714

6.  Renal mitochondrial cytopathies.

Authors:  Francesco Emma; Giovanni Montini; Leonardo Salviati; Carlo Dionisi-Vici
Journal:  Int J Nephrol       Date:  2011-07-27

Review 7.  Renal involvement in mitochondrial cytopathies.

Authors:  Francesco Emma; Enrico Bertini; Leonardo Salviati; Giovanni Montini
Journal:  Pediatr Nephrol       Date:  2011-06-09       Impact factor: 3.714

8.  Compound heterozygous RMND1 gene variants associated with chronic kidney disease, dilated cardiomyopathy and neurological involvement: a case report.

Authors:  Asheeta Gupta; Isabel Colmenero; Nicola K Ragge; Emma L Blakely; Langping He; Robert McFarland; Robert W Taylor; Julie Vogt; David V Milford
Journal:  BMC Res Notes       Date:  2016-06-27
  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.