Surgical Management of Facial Features of Robinow Syndrome: A Case Report | Zendy

Aida M. Mossaad | Zendy; Moustapha A Abdelrahman | Zendy; Mostafa Ibrahim | Zendy; Hatem H. Al Ahmady | Zendy

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Surgical Management of Facial Features of Robinow Syndrome: A Case Report

Author(s) -

Aida M. Mossaad,

Moustapha A Abdelrahman,

Mostafa Ibrahim,

Hatem H. Al Ahmady

Publication year - 2018

Publication title -

open access macedonian journal of medical sciences

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.288

H-Index - 17

ISSN - 1857-9655

DOI - 10.3889/oamjms.2018.129

Subject(s) - medicine , macrocephaly , hypertelorism , ectrodactyly , frontal bossing , pinna , chin , short stature , nose , physical examination , micropenis , anatomy , surgery , dermatology , hypospadias , ectodermal dysplasia , pediatrics

Robinow Syndrome is an extremely rare genetic disorder characterised by abnormalities in head, face and external genitalia. This disorder exists in dominant pattern with moderate symptoms and recessive pattern with more physical and skeletal abnormalities. It was first introduced by Menihard Robinow in 1969. It was related to chromosome 9q22 ROR2 gene related to bone and cartilage growth aspects.

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