Literature DB >> 15057123

Hypertrichosis, hyperkeratosis, abnormal corpus callosum, mental retardation and dysmorphic features in three unrelated females.

Minna H Pöyhönen1, Maarit M Peippo, Leena K Valanne, Kirsti E Kuokkanen, Susanna M Koskela, Oliver Bartsch, Sasan Rasi, Glenis J Wiebe, Marketta Kähkönen, Helena A Kääriäinen.   

Abstract

We report three unrelated patients with hypertrichosis, mild to moderate mental retardation, and dysmorphic facial features including low anterior hairline, thick arched eyebrows, nose with broad tip and columella below alae nasi, short philtrum, thick drooping lower lip and simple posteriorly rotated ears. They also had rough skin with hyperkeratotic plaques. Feet and finger tips were broad. All of them had personality problems like aggressiveness, stubborn temperament or tendency to withdraw. Brain MRI showed thick and short corpus callosum. We believe that these patients represent a new syndrome of unknown aetiology.

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Year:  2004        PMID: 15057123     DOI: 10.1097/00019605-200404000-00006

Source DB:  PubMed          Journal:  Clin Dysmorphol        ISSN: 0962-8827            Impact factor:   0.816


  6 in total

1.  Microstructural changes in thickened corpus callosum in children: contribution of magnetic resonance diffusion tensor imaging.

Authors:  Laura Merlini; Mehrak Anooshiravani; Aikaterini Kanavaki; Sylviane Hanquinet
Journal:  Pediatr Radiol       Date:  2014-12-03

2.  DNA sequencing of CREBBP demonstrates mutations in 56% of patients with Rubinstein-Taybi syndrome (RSTS) and in another patient with incomplete RSTS.

Authors:  Oliver Bartsch; Stefanie Schmidt; Marion Richter; Susanne Morlot; Eva Seemanová; Glenis Wiebe; Sasan Rasi
Journal:  Hum Genet       Date:  2005-07-14       Impact factor: 4.132

Review 3.  Corpus callosum thickness in children: an MR pattern-recognition approach on the midsagittal image.

Authors:  Savvas Andronikou; Tanyia Pillay; Lungile Gabuza; Nasreen Mahomed; Jaishree Naidoo; Linda Tebogo Hlabangana; Vicci du Plessis; Sanjay P Prabhu
Journal:  Pediatr Radiol       Date:  2014-08-31

4.  The HHID syndrome of hypertrichosis, hyperkeratosis, abnormal corpus callosum, intellectual disability, and minor anomalies is caused by mutations in ARID1B.

Authors:  Markus Zweier; Maarit M Peippo; Minna Pöyhönen; Helena Kääriäinen; Anaïs Begemann; Pascal Joset; Beatrice Oneda; Anita Rauch
Journal:  Am J Med Genet A       Date:  2017-03-21       Impact factor: 2.802

5.  Thick Corpus Callosum in Children.

Authors:  Aviv Schupper; Osnat Konen; Ayelet Halevy; Rony Cohen; Sharon Aharoni; Avinoam Shuper
Journal:  J Clin Neurol       Date:  2017-04       Impact factor: 3.077

6.  A new family with spastic paraplegia type 51 and novel mutations in AP4E1.

Authors:  Izabela Winkler; Paweł Miotła; Monika Lejman; Aleksandra Pietrzyk; Magdalena Kacprzak; Marcin Kubiak; Agnieszka Sobczyńska-Tomaszewska; Maciej Skrzypczak; Ilona Jaszczuk
Journal:  BMC Med Genomics       Date:  2021-05-18       Impact factor: 3.063

  6 in total

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