A rare progressive neurological condition that can affect development, movement and participation in everyday activities. 

A genetic neurodevelopmental condition commonly associated with developmental delay, movement and balance challenges, and communication differences. 

Autism Spectrum Disorder (ASD) can affect communication, social interaction, sensory processing, and daily routines in different ways for each person. Learn more about common supports and how allied health can help build participation and independence. 

A condition present from birth involving multiple joint contractures, which can affect movement, mobility and functional independence. 

A structural condition affecting the brain and upper spinal canal that may contribute to pain, balance, coordination or neurological symptoms. 

A rare neurological disorder that can affect development, movement, tone and functional skills over time. 

A rare genetic condition that can affect brain development, vision, seizures and developmental progress. 

A rare genetic neurological condition that may impact development, movement, muscle tone and communication. 

A rare genetic condition that can affect vision, hearing, growth and multiple body systems across the lifespan. 

A rare inherited neurological disorder that can lead to progressive changes in movement, communication, vision and daily function. 

A complex genetic syndrome that may affect hearing, vision, balance, feeding, development and participation in daily life. 

A rare inherited neurological condition that affects brain development and can impact movement, tone and functional skills. 

A congenital difference affecting the lip and/or palate that may impact feeding, speech development and oral function. 

A rare genetic condition associated with developmental delay, intellectual disability and musculoskeletal differences. 

A congenital condition where part or all of a limb does not form typically, affecting mobility, function and independence. 

A genetic condition associated with developmental delay, communication challenges and varying physical and functional needs. 

A rare genetic disorder that can affect growth, development, mobility and neurological function. 

A rare genetic condition that may involve developmental delay, low muscle tone and coordination or communication challenges. 

A genetic syndrome that can affect growth, development, communication and motor skills, with support needs varying widely. 

A genetic condition that primarily affects the lungs and digestive system and may impact endurance, physical function and daily routines. 

A congenital brain malformation that can affect balance, coordination, muscle tone and developmental progress. 

A genetic condition that can affect heart, immune and developmental health, with support needs varying across individuals. 

A genetic condition caused by an extra chromosome 21, commonly associated with developmental delay, low muscle tone and learning differences. 

A rare chromosomal condition associated with significant medical and developmental challenges and complex support needs. 

A genetic condition that can affect learning, behaviour, sensory processing and communication. 

A neurodevelopmental condition related to prenatal alcohol exposure that can affect learning, behaviour, emotional regulation and daily function. 

A condition linked to prenatal exposure to certain anti-seizure medications, which may affect growth and development. 

Rare inherited metabolic conditions that can affect the brain and body, impacting movement, development and medical needs. 

A rare progressive neurological disorder that can affect movement, tone, coordination and functional ability over time. 

A rare inherited metabolic disorder that can affect growth, joints, mobility, breathing and daily function. 

A rare inherited metabolic condition that may affect movement, development, endurance and multiple body systems. 

A condition involving excess fluid in the brain that may affect development, mobility, coordination and functional skills. 

A condition involving differences in learning, reasoning and adaptive functioning, with support needs varying from person to person. 

A rare genetic condition that commonly affects balance, coordination, eye movements and developmental progress. 

A rare genetic syndrome associated with developmental delay, low muscle tone and a range of physical and functional support needs. 

A rare inherited neurological condition that can affect movement, tone, feeding and developmental abilities. 

A rare inherited metabolic disorder that can affect movement, muscle tone, behaviour and daily functioning. 

A rare progressive neurological condition that can impact movement, breathing, feeding and developmental skills. 

A rare inherited metabolic disorder that can affect joints, mobility, growth and functional independence. 

A rare genetic disorder affecting copper metabolism that can impact neurological development, muscle tone and growth. 

A rare inherited condition that affects bone and joint development, often impacting mobility and endurance. 

A genetic connective tissue condition that can affect joints, posture, fatigue and physical activity tolerance. 

A condition where head size is smaller than expected, sometimes associated with developmental and neurological differences. 

Genetic conditions that can affect the nervous system, hearing, balance, pain and function in different ways. 

A genetic condition that may affect growth, motor development, heart health and learning. 

A group of rare inherited metabolic disorders that can affect the brain, movement and organ function. 

A genetic condition affecting bone strength, often associated with fractures, mobility challenges and physical support needs. 

A rare chromosomal condition associated with complex medical and developmental needs. 

A rare genetic neurological disorder that can affect muscle tone, movement, coordination and development. 

A rare inherited metabolic condition requiring dietary management to support healthy development and function. 

A rare inherited condition that can affect muscles, breathing and physical endurance. 

A complex genetic condition often involving low muscle tone, developmental delay, feeding changes and ongoing support needs across childhood and beyond. 

A neurological developmental disorder that primarily affects girls and can impact hand use, communication, mobility and daily function. 

A rare inherited metabolic disorder that can affect development, behaviour, sleep and progressive neurological function. 

A rare genetic condition associated with developmental delay, physical differences and varied support needs. 

A genetic developmental disorder often associated with communication, behaviour, sleep and sensory regulation challenges. 

A congenital condition affecting the spine and nervous system, which may impact mobility, continence and daily function. 

A genetic neuromuscular condition that causes muscle weakness and can affect mobility, breathing and function. 

A rare inherited metabolic condition that can affect joints, mobility, vision and daily activities. 

A rare inherited metabolic disorder that may impact development, mobility and multiple body systems. 

A rare genetic condition associated with growth restriction, developmental delay and complex support needs. 

A rare neurological condition that can affect the brain, skin and eyes, with possible impacts on seizures, movement and development. 

A rare inherited neurological disorder that progressively affects movement, development and functional skills. 

A rare inherited metabolic condition that can affect neurological function, movement and development. 

A chromosomal condition affecting females that may impact growth, development and some aspects of physical function. 

A genetic condition that can affect the brain and other organs, often involving seizures, development and learning differences. 

A rare chromosomal condition associated with significant developmental and medical complexity, with support needs varying widely. 

A rare inherited neurological disorder that progressively affects movement, development and function. 

A group of congenital differences affecting multiple body systems, often requiring coordinated multidisciplinary support. 

A genetic condition associated with developmental differences, learning needs, motor challenges and unique social strengths. 

A rare genetic condition that can affect vision, hearing, neurological function and long-term health needs. 

We support children, adults and older adults with disability, injury, chronic conditions, developmental concerns, communication needs, mobility challenges and rehabilitation goals.

Find the right support by discipline, including physiotherapy, occupational therapy, speech therapy, exercise physiology and other allied health services.

Palms Physiotherapy & Allied Health offers a range of therapy services and specialised supports. You can browse by therapy area, explore specialised services, or learn more about the facilities and equipment we use in-clinic .

We support children, adults and older adults with disability, injury, chronic conditions, developmental concerns, communication needs, mobility challenges and rehabilitation goals.