Literature DB >> 6107045

A new form of X-linked mental retardation with growth retardation, deafness, and microgenitalism.

R C Juberg, I Marsidi.   

Abstract

The proband and two maternal uncles were similarly affected by a unique constellation of mental retardation and physical abnormalities. There were severe retardation, growth less than the third percentile, and significantly delayed bone age. They manifested deafness, a flat nasal bridge, several ocular abnormalities, and a rudimentary scrotum with cryptorchidism, and one had a small penis. The proband also had onychodystrophy of his fingers and toes. Their birth weights and lengths were less than expected. No chromosomal or biochemical abnormality was detected. Both uncles died, but the proband is healthy at 4 years. Their phenotype is distinguished from other forms of X-linked mental retardation and appears to be a new syndrome.

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Year:  1980        PMID: 6107045      PMCID: PMC1686104     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  16 in total

1.  X-linked mental retardation associated with macro-orchidism.

Authors:  G Turner; C Eastman; J Casey; A McLeay; P Procopis; B Turner
Journal:  J Med Genet       Date:  1975-12       Impact factor: 6.318

2.  X-linked mental retardation and-or hydrocephalus.

Authors:  K Fried
Journal:  Clin Genet       Date:  1972       Impact factor: 4.438

3.  X-linked recessively inherited non-specific mental retardation. Report of a large family.

Authors:  J Deroover; J P Fryns; C Parloir; H Van den Berghe
Journal:  Ann Genet       Date:  1977-12

4.  X-linked skeletal dysplasia with mental retardation.

Authors:  J C Christian; E A DeMyer Franken; J S Huff; S Khairi; T Reed
Journal:  Clin Genet       Date:  1977-02       Impact factor: 4.438

5.  Marker X chromosomes, mental retardation and macro-orchidism.

Authors:  G Turner; R Till; A Daniel
Journal:  N Engl J Med       Date:  1978-12-28       Impact factor: 91.245

6.  Carrier detection in X-linked mental retardation.

Authors:  G R Sutherland
Journal:  Med J Aust       Date:  1978-12-30       Impact factor: 7.738

7.  Sex-linked spastic paraplegia.

Authors:  H S Baar; A M Gabriel
Journal:  Am J Ment Defic       Date:  1966-07

8.  X-linked nonspecific mental retardation. Report of a large kindred.

Authors:  K M Yarbrough; P N Howard-Peebles
Journal:  Clin Genet       Date:  1976-02       Impact factor: 4.438

9.  Familial X-linked mental retardation with an X chromosome abnormality.

Authors:  J Harvey; C Judge; S Wiener
Journal:  J Med Genet       Date:  1977-02       Impact factor: 6.318

10.  X-linked hypogonadism, gynecomastia, mental retardation, short stature, and obesity--a new syndrome.

Authors:  S B Vasquez; D L Hurst; J F Sotos
Journal:  J Pediatr       Date:  1979-01       Impact factor: 4.406

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  11 in total

1.  A novel mutation in the putative DNA helicase XH2 is responsible for male-to-female sex reversal associated with an atypical form of the ATR-X syndrome.

Authors:  A Ion; L Telvi; J L Chaussain; F Galacteros; J Valayer; M Fellous; K McElreavey
Journal:  Am J Hum Genet       Date:  1996-06       Impact factor: 11.025

Review 2.  X linked mental retardation.

Authors:  I A Glass
Journal:  J Med Genet       Date:  1991-06       Impact factor: 6.318

3.  HUWE1 variants cause dominant X-linked intellectual disability: a clinical study of 21 patients.

Authors:  Stéphanie Moortgat; Siren Berland; Ingvild Aukrust; Isabelle Maystadt; Laura Baker; Valerie Benoit; Alfonso Caro-Llopis; Nicola S Cooper; François-Guillaume Debray; Laurence Faivre; Thatjana Gardeitchik; Bjørn I Haukanes; Gunnar Houge; Emma Kivuva; Francisco Martinez; Sarju G Mehta; Marie-Cécile Nassogne; Nina Powell-Hamilton; Rolph Pfundt; Monica Rosello; Trine Prescott; Pradeep Vasudevan; Barbara van Loon; Christine Verellen-Dumoulin; Alain Verloes; Charlotte von der Lippe; Emma Wakeling; Andrew O M Wilkie; Louise Wilson; Amy Yuen; Ddd Study; Karen J Low; Ruth A Newbury-Ecob
Journal:  Eur J Hum Genet       Date:  2017-11-27       Impact factor: 4.246

4.  X-linked mental retardation: in pursuit of a gene map.

Authors:  C E Schwartz
Journal:  Am J Hum Genet       Date:  1993-06       Impact factor: 11.025

5.  The Juberg-Marsidi syndrome maps to the proximal long arm of the X chromosome (Xq12-q21).

Authors:  P Saugier-Veber; V Abadie; A Moncla; M Mathieu; C Piussan; C Turleau; J F Mattei; A Munnich; S Lyonnet
Journal:  Am J Hum Genet       Date:  1993-06       Impact factor: 11.025

6.  A variant of the fra(X) syndrome.

Authors:  E M Bühler; F Hadziselimovic; U Pira
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

7.  X linked mental retardation: a family with a separate syndrome?

Authors:  E M Thompson; A Gordon; M Baraitser
Journal:  J Med Genet       Date:  1989-06       Impact factor: 6.318

8.  Xp11.22 deletions encompassing CENPVL1, CENPVL2, MAGED1 and GSPT2 as a cause of syndromic X-linked intellectual disability.

Authors:  Christina Grau; Molly Starkovich; Mahshid S Azamian; Fan Xia; Sau Wai Cheung; Patricia Evans; Alex Henderson; Seema R Lalani; Daryl A Scott
Journal:  PLoS One       Date:  2017-04-17       Impact factor: 3.240

9.  HUWE1 mutations in Juberg-Marsidi and Brooks syndromes: the results of an X-chromosome exome sequencing study.

Authors:  Michael J Friez; Susan Sklower Brooks; Roger E Stevenson; Michael Field; Monica J Basehore; Lesley C Adès; Courtney Sebold; Stephen McGee; Samantha Saxon; Cindy Skinner; Maria E Craig; Lucy Murray; Richard J Simensen; Ying Yzu Yap; Marie A Shaw; Alison Gardner; Mark Corbett; Raman Kumar; Matthias Bosshard; Barbara van Loon; Patrick S Tarpey; Fatima Abidi; Jozef Gecz; Charles E Schwartz
Journal:  BMJ Open       Date:  2016-04-29       Impact factor: 2.692

10.  Targeted Next-Generation Sequencing in Patients with Suggestive X-Linked Intellectual Disability.

Authors:  Nekane Ibarluzea; Ana Belén de la Hoz; Olatz Villate; Isabel Llano; Intzane Ocio; Itxaso Martí; Miriam Guitart; Elisabeth Gabau; Fernando Andrade; Blanca Gener; María-Isabel Tejada
Journal:  Genes (Basel)       Date:  2020-01-02       Impact factor: 4.096

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