Literature DB >> 7717418

Craniodigital syndromes: report of a child with Filippi syndrome and discussion of differential diagnosis.

H V Toriello1, J V Higgins.   

Abstract

We describe a boy with low birth weight, congenital microcephaly, multiple minor facial anomalies, cleft palate, soft tissue syndactyly of fingers and toes, and moderate to severe mental retardation. Literature review suggested 6 possible diagnoses, including Scott craniodigital syndrome, Chitayat syndrome, Filippi syndrome, Zerres syndrome, Kelly syndrome, and Woods syndrome. Each has as part of the phenotype craniofacial anomalies and soft tissue syndactyly of fingers and toes; and superficially, distinction among the 6 may be difficult. However, based on the phenotype analysis we performed, we conclude that our patient has Filippi syndrome, and thus is the first reported case from the United States.

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Year:  1995        PMID: 7717418     DOI: 10.1002/ajmg.1320550210

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  3 in total

1.  Filippi Syndrome: Report of a Rare Case.

Authors:  Lata Goyal; Jagdish Prasad Goyal; Bhanu Kiran Bhakhri; Ashi Chug
Journal:  J Clin Diagn Res       Date:  2015-12-01

2.  De novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway.

Authors:  Maria Asif; Emrah Kaygusuz; Marwan Shinawi; Anna Nickelsen; Tzung-Chien Hsieh; Prerana Wagle; Birgit S Budde; Jennifer Hochscherf; Uzma Abdullah; Stefan Höning; Christian Nienberg; Dirk Lindenblatt; Angelika A Noegel; Janine Altmüller; Holger Thiele; Susanne Motameny; Nicole Fleischer; Idan Segal; Lynn Pais; Sigrid Tinschert; Nadra Nasser Samra; Juliann M Savatt; Natasha L Rudy; Chiara De Luca; Susan M White; Peter Krawitz; Anna C E Hurst; Karsten Niefind; Joachim Jose; Francesco Brancati; Peter Nürnberg; Muhammad Sajid Hussain
Journal:  HGG Adv       Date:  2022-04-18

Review 3.  Filippi syndrome: a new case with skeletal abnormalities.

Authors:  D Héron; T Billette de Villemeur; A Munnich; S Lyonnet
Journal:  J Med Genet       Date:  1995-08       Impact factor: 6.318

  3 in total

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