Syndrome Sheets
Resources for clinicians -syndrome specific information and current research
The SSBP have created a portfolio of Syndrome Sheets, written by members with specific expertise in the treatment of a variety of syndromes.
The information contained in these syndrome sheets is aimed at clinicians, is for guidance only, and does not constitute a diagnostic tool. Many syndromes manifest in varying degrees of severity, and this information is not intended to inform patients of a specific prognosis.
The SSBP strongly recommends patients to follow the advice and direction of their clinical team, who will be most able to assess their individual situation
Syndrome Sheets represent the views of the authors who kindly prepared them, and not necessarily those of the SSBP.
Latest Updates (2021)
The following syndrome sheets have been updated in 2021:
- Cri du Chat Syndrome
- Mowat-Wilson Syndrome
- Noonan Syndrome
- Rett Syndrome (RTT)
- Turner Syndrome
The following syndrome sheets were updated in 2020:
- Triple-X Syndrome (47,XXX)
The following syndrome sheets were updated in 2019:
- CHARGE Syndrome
- Coffin-Lowry Syndrome
- Coffin Siris Syndrome
- Cornelia de Lange Syndrome
- Down Syndrome
- Fetal Alcohol Syndrome
- Fragile X Syndrome
- Neurofibromatosis Type 1 (NF1)
- Prader-Willi Syndrome
- Rubenstein-Taybi Syndrome
- Tuberous Sclerosis Complex
- Williams Syndrome
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The Society for the Study of Behavioural Phenotypes (SSBP)
The Society for the Study of Behavioural Phenotypes (SSBP) is an international, interdisciplinary research society for studying the development, learning and behaviours of individuals with genetic disorders and ways of helping to improve lives. The society is registered as a charity in the UK (No. 1013849) and was set up in 1987.
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