Articles liés à COFFIN–LOWRY SYNDROME: An X-Linked Genetic Disorder...

COFFIN–LOWRY SYNDROME: An X-Linked Genetic Disorder of Cognitive, Craniofacial, and Skeletal Development - Couverture souple

Light, Space; Zion, Princess; SMITH, ELIANCE

 
9798190869309: COFFIN–LOWRY SYNDROME: An X-Linked Genetic Disorder of Cognitive, Craniofacial, and Skeletal Development
Couverture souple
ISBN 13 : 9798190869309
Editeur : Independently published, 2026

Synopsis

Somewhere right now, a parent is hearing the words "Coffin–Lowry syndrome" for the very first time and driving home with more questions than answers.

This book exists to change that.

Coffin–Lowry Syndrome is the comprehensive, evidence-based guide to this rare genetic disorder that families and caregivers need when it impacts their lives. From physical traits that suggest it may be the cause to diagnosis, treatment, RPS6KA3, and beyond, this book provides trusted medical information and advice in one convenient resource.

Inside, you'll learn:

How Coffin–Lowry syndrome is diagnosed and why early recognition matters
The genetics behind it, explained in plain language
What effective treatment and multidisciplinary care actually look like
How to support communication, learning, and development at every age
What the latest research says about outcomes and quality of life
The history of the condition and the community built around it

Written for parents, special educators, genetic counselors, and clinicians alike, this book turns an overwhelming diagnosis into a clear path forward.

Because understanding is the first step toward truly supporting the person behind the diagnosis.

Les informations fournies dans la section « Synopsis » peuvent faire référence à une autre édition de ce titre.

Éditeur
Independently published
Date d'édition
2026
Langue
anglais
ISBN 13 
9798190869309
Reliure
Paperback
Nombre de pages
59
Coordonnées du fabricant
non disponible
Personne responsable
non disponible