Literature DB >> 1127528

The inheritance of the Aarskog facial-digital-genital syndrome.

P Berman, C Desjardins, F C Fraser.   

Abstract

Prominent physical features of the Aarskog syndrome are short stature, telecanthus, ptosis, short broad nose, long philtrum, thin upper vermilion border and pouty lower lip, low-set jug-handle ears, short broad hands with clawlike positioning of the fingers, broad feet with bulbous toes, ventral scrotal folds, cryptorchidism, and hernias. Four families with 20 affected males are reported. Pedigree analysis is compatible with X-linked recessive inheritance with occasional partial expression in heterozygote females. The fact that seven sons, all unaffected, have been born to affected males argues against the alternative hypothesis of autosomal sex-influenced inheritance.

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Year:  1975        PMID: 1127528     DOI: 10.1016/s0022-3476(75)80219-8

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  7 in total

1.  Aarskog syndrome.

Authors:  M E Porteous; D R Goudie
Journal:  J Med Genet       Date:  1991-01       Impact factor: 6.318

2.  An autosomal recessive disorder with retardation of growth, mental deficiency, ptosis, pectus excavatum and camptodactyly.

Authors:  F Khaldi; B Bennaceur; A Hammou; M Hamza; H A Gharbi
Journal:  Pediatr Radiol       Date:  1988

3.  Aarskog syndrome with isolated growth hormone deficiency.

Authors:  M Kodama; S Fujimoto; T Namikawa; I Matsuda
Journal:  Eur J Pediatr       Date:  1981-02       Impact factor: 3.183

4.  Aarskog's syndrome.

Authors:  C Berry; J Cree; T Mann
Journal:  Arch Dis Child       Date:  1980-09       Impact factor: 3.791

5.  Intelligence and development in Aarskog syndrome.

Authors:  L J Logie; M E Porteous
Journal:  Arch Dis Child       Date:  1998-10       Impact factor: 3.791

6.  New autosomal recessive faciodigitogenital syndrome.

Authors:  A S Teebi; K K Naguib; S Al-Awadi; Q A Al-Saleh
Journal:  J Med Genet       Date:  1988-06       Impact factor: 6.318

7.  Aarskog-Scott syndrome: clinical and molecular characterisation of a family with the coexistence of a novel FGD1 mutation and 16p13.11-p12.3 microduplication.

Authors:  Piero Pavone; Silvia Marino; Antonino Maniaci; Salvatore Cocuzza
Journal:  BMJ Case Rep       Date:  2020-06-30
  7 in total

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