Search

Search Results
Results 1 - 6 of 6 for Pectus excavatum
  • Health - 25 May 2021
    Noonan syndrome is a heterogeneous, but clinically recognizable, multiple congenital anomaly syndrome.
  • Health - 23 Mar 2021
    Noonan syndrome is a common autosomal dominant multiple congenital anomaly syndrome.
  • Health - 9 Feb 2021
    Noonan syndrome is one of the most common non-chromosomal disorders in children with congenital heart disease.
  • Health - 19 May 2022
    Bannayan-Riley-Ruvalcaba Syndrome (BRRS) is a congenital genetic condition defined by a group of characteristic features. This article discusses the condition in depth.
  • Health - 26 Feb 2019
    Becker nevus syndrome, or hairy epidermal nevus syndrome, was first described by Happle in 1949, as an association of Becker nevus with breast hypoplasia on one side of the body, and ipsilateral...
  • Health - 21 Feb 2023
    A genetic disorder caused by the gene mutation FGD1 (faciogenital dysplasia) can result in a disorder called Aarskog syndrome, or Aarskog-Scott syndrome.

While we only use edited and approved content for Azthena answers, it may on occasions provide incorrect responses. Please confirm any data provided with the related suppliers or authors. We do not provide medical advice, if you search for medical information you must always consult a medical professional before acting on any information provided.

Your questions, but not your email details will be shared with OpenAI and retained for 30 days in accordance with their privacy principles.

Please do not ask questions that use sensitive or confidential information.

Read the full Terms & Conditions.