Literature DB >> 3179424

Rapp-Hodgkin syndrome: observations on ten cases and characteristic hair changes (pili canaliculi).

C F Salinas1, G M Montes.   

Abstract

We have reported on six personally examined patients with Rapp Hodgkin syndrome and four additional family members with documentation suggesting strongly that they also were affected with the disorder. Clinical manifestations observed in our patients include cleft lip/palate/uvula, ectodermal dysplasia, and hypospadias in males. The ectodermal dysplasia manifests through uncombable, sparse, wiry hair; alopecia in adulthood; hypodontia; hypohidrosis; and dysplastic nails. In addition, ptosis, atretric ear canals, and dysplastic eustachian orifices are suggested as other manifestations of the disorder.

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Mesh:

Year:  1988        PMID: 3179424

Source DB:  PubMed          Journal:  Birth Defects Orig Artic Ser        ISSN: 0547-6844


  9 in total

1.  Light microscopic examination of scalp hair samples as an aid in the diagnosis of paediatric disorders: retrospective review of more than 300 cases from a single centre.

Authors:  V V Smith; G Anderson; M Malone; N J Sebire
Journal:  J Clin Pathol       Date:  2005-12       Impact factor: 3.411

2.  Cephalometric analysis of Rapp-Hodgkin syndrome.

Authors:  T C Hart; S Kyrkanides
Journal:  J Med Genet       Date:  1994-10       Impact factor: 6.318

3.  Twenty-four cases of the EEC syndrome: clinical presentation and management.

Authors:  P W Buss; H E Hughes; A Clarke
Journal:  J Med Genet       Date:  1995-09       Impact factor: 6.318

Review 4.  Modeling AEC-New approaches to study rare genetic disorders.

Authors:  Peter J Koch; Jason Dinella; Mary Fete; Elaine C Siegfried; Maranke I Koster
Journal:  Am J Med Genet A       Date:  2014-03-24       Impact factor: 2.802

5.  Rapp Hodgkin Syndrome.

Authors:  Manas Chatterjee; Shekhar Neema; Sweta Mukherjee
Journal:  Indian Dermatol Online J       Date:  2017 May-Jun

6.  Ocular manifestations of ectodermal dysplasia.

Authors:  Daphna Landau Prat; William R Katowitz; Alanna Strong; James A Katowitz
Journal:  Orphanet J Rare Dis       Date:  2021-05-01       Impact factor: 4.303

7.  Familial cleft tongue caused by a unique translation initiation codon variant in TP63.

Authors:  Julia Schmidt; Gudrun Schreiber; Janine Altmüller; Holger Thiele; Peter Nürnberg; Yun Li; Silke Kaulfuß; Rudolf Funke; Bernd Wilken; Gökhan Yigit; Bernd Wollnik
Journal:  Eur J Hum Genet       Date:  2021-10-11       Impact factor: 4.246

8.  Use of FACIAL ARTERY MUSCULOMUCOSAL and Turbinate Flaps for Rapp Hodgkin Syndrome.

Authors:  Mahdy Saboury; Noor Ahmad Latifi; Shahriar Saboury; Moosa Saboury
Journal:  World J Plast Surg       Date:  2022-07

9.  Spectrum of Genetic Variants Associated with Anterior Segment Dysgenesis in South Florida.

Authors:  Saradadevi Thanikachalam; Elizabeth Hodapp; Ta C Chang; Dayna Morel Swols; Filiz B Cengiz; Shengru Guo; Mohammad F Zafeer; Serhat Seyhan; Guney Bademci; William K Scott; Alana Grajewski; Mustafa Tekin
Journal:  Genes (Basel)       Date:  2020-03-26       Impact factor: 4.096

  9 in total

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