Literature DB >> 20362700

Familial occurrence of ptosis, nasal speech, prominent ears, hand anomalies and learning problems.

Elga F Belligni1, Raoul C M Hennekam.   

Abstract

We describe a four-generation family in whom 5 members show the combination of a large head, ptosis, nasal speech that sometimes goes along with a cleft palate, full cheeks, small mouth, and prominent ears, and who also have learning problems. We evaluated three affected members in detail and found them to have in addition a partial cutaneous syndactyly between the third and fourth fingers, an increased distance between second and third finger, and a decreased smell. We have not been unable to find other patients described in literature with the same combination of features, and suggest this to represent a hitherto unrecognizable entity. Pattern of inheritance is likely to be autosomal dominant. Copyright 2010 Elsevier Masson SAS. All rights reserved.

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Year:  2010        PMID: 20362700     DOI: 10.1016/j.ejmg.2010.03.009

Source DB:  PubMed          Journal:  Eur J Med Genet        ISSN: 1769-7212            Impact factor:   2.708


  2 in total

1.  Characterization of a 8q21.11 microdeletion syndrome associated with intellectual disability and a recognizable phenotype.

Authors:  María Palomares; Alicia Delicado; Elena Mansilla; María Luisa de Torres; Elena Vallespín; Luis Fernandez; Victor Martinez-Glez; Sixto García-Miñaur; Julián Nevado; Fernando Santos Simarro; Victor L Ruiz-Perez; Sally Ann Lynch; Freddie H Sharkey; Ann-Charlotte Thuresson; Göran Annerén; Elga F Belligni; María Luisa Martínez-Fernández; Eva Bermejo; Beata Nowakowska; Anna Kutkowska-Kazmierczak; Ewa Bocian; Ewa Obersztyn; María Luisa Martínez-Frías; Raoul C M Hennekam; Pablo Lapunzina
Journal:  Am J Hum Genet       Date:  2011-07-28       Impact factor: 11.025

2.  8q21.11 microdeletion syndrome: Delineation of HEY1 as a candidate gene in neurodevelopmental and cardiac defects.

Authors:  Ikhlas Ben Ayed; Amal Bouzid; Fatma Kammoun; Amal Souissi; Olfa Jallouli; Salma Mallouli; Souhir Guidara; Salma Loukil; Hajer Aloulou; Fida Jbeli; Sahar Aouichaoui; Dorra Abid; Fatma Abdelhedi; Chahnez Triki; Hassen Kamoun; Saber Masmoudi
Journal:  Mol Genet Genomic Med       Date:  2021-09-22       Impact factor: 2.183

  2 in total

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