Literature DB >> 3236353

Autosomal dominant isolated ('uncomplicated') microcephaly.

P Merlob1, D Steier, S H Reisner.   

Abstract

A large family (13 affected members in three generations) is reported in which isolated microcephaly occurred without any other dysmorphic or neurological abnormalities. The family pedigree confirms the autosomal dominant mode of inheritance with incomplete penetrance, including one example of male to male transmission and the occurrence of a non-manifesting heterozygote resulting in a 'skipped generation'. There is considerable variation in the phenotypic expression of autosomal dominant microcephaly. This isolated (uncomplicated) type of microcephaly should be distinguished from other well defined, dominantly inherited forms of microcephaly.

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Year:  1988        PMID: 3236353      PMCID: PMC1051578          DOI: 10.1136/jmg.25.11.750

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  13 in total

1.  A clinical and genetical study of microcephaly.

Authors:  J A BOOK; J W SCHUT; S C REED
Journal:  Am J Ment Defic       Date:  1953-04

2.  Head circumference from birth to eighteen years. Practical composite international and interracial graphs.

Authors:  G Nellhaus
Journal:  Pediatrics       Date:  1968-01       Impact factor: 7.124

3.  Intrauterine growth of live-born Caucasian infants at sea level: standards obtained from measurements in 7 dimensions of infants born between 25 and 44 weeks of gestation.

Authors:  R Usher; F McLean
Journal:  J Pediatr       Date:  1969-06       Impact factor: 4.406

4.  Anthropometric measurements of the newborn infant (27 to 41 gestational weeks).

Authors:  P Merlob; Y Sivan; S H Reisner
Journal:  Birth Defects Orig Artic Ser       Date:  1984

5.  Silent microcephaly: a distinct autosomal dominant trait.

Authors:  M L Ramírez; F Rivas; J M Cantú
Journal:  Clin Genet       Date:  1983-04       Impact factor: 4.438

6.  Dominant inheritance of microcephaly with short stature.

Authors:  B K Burton
Journal:  Clin Genet       Date:  1981-07       Impact factor: 4.438

7.  Chorio-retinal dysplasia, microcephaly and mental retardation. An autosomal dominant syndrome.

Authors:  R Tenconi; M Clementi; G B Moschini; G Casara; C Baccichetti
Journal:  Clin Genet       Date:  1981-11       Impact factor: 4.438

8.  Little heads: inheritance and early detection.

Authors:  F Hecht; J V Kelly
Journal:  J Pediatr       Date:  1979-11       Impact factor: 4.406

9.  Dominantly inherited syndrome of microcephaly and congenital lymphedema.

Authors:  A K Leung
Journal:  Clin Genet       Date:  1985-06       Impact factor: 4.438

10.  Autosomal dominant microcephaly.

Authors:  R H Haslam; D W Smith
Journal:  J Pediatr       Date:  1979-11       Impact factor: 4.406

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  4 in total

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Authors:  Neerja Gupta; Vishal Vishnu Tewari; Manoj Kumar; Nitika Langeh; Aditi Gupta; Pallavi Mishra; Punit Kaur; Vedam Ramprasad; Sakthivel Murugan; Reema Kumar; Manisha Jana; Madhulika Kabra
Journal:  Metab Brain Dis       Date:  2017-08-03       Impact factor: 3.584

2.  Zika virus: accurate terminology matters.

Authors:  Edwin P Kirk
Journal:  Nature       Date:  2016-03-10       Impact factor: 49.962

3.  Microcephaly and congenital nephrotic syndrome owing to diffuse mesangial sclerosis: an autosomal recessive syndrome.

Authors:  B Z Garty; B Eisenstein; J Sandbank; S Kaffe; R Dagan; N Gadoth
Journal:  J Med Genet       Date:  1994-02       Impact factor: 6.318

4.  Primary microcephaly case from the Karachay-Cherkess Republic poses an additional support for microcephaly and Seckel syndrome spectrum disorders.

Authors:  Andrey V Marakhonov; Fedor A Konovalov; Amin Kh Makaov; Tatyana A Vasilyeva; Vitaly V Kadyshev; Varvara A Galkina; Elena L Dadali; Sergey I Kutsev; Rena A Zinchenko
Journal:  BMC Med Genomics       Date:  2018-02-13       Impact factor: 3.063

  4 in total

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