Sprouting Up Therapy

Sprouting Up Therapy Contact information, map and directions, contact form, opening hours, services, ratings, photos, videos and announcements from Sprouting Up Therapy, Physical therapist, Montgomery, TX.

Our mission is to improve the health and enrich the lives of individuals by working one-on-one to promote independent function and social participation through gross motor skills including strengthening, flexibility, balance, and mobility.

Rett syndromeIs a rare, severe neurodevelopmental disorder caused by genetic mutation in MECP2 gene on X chromosomeOccur...
03/29/2026

Rett syndrome

Is a rare, severe neurodevelopmental disorder caused by genetic mutation in MECP2 gene on X chromosome
Occurs almost exclusively in females; incidence 1 in 10,000 births, boys die shortly after birth. It causes significant, sudden loss of purposeful hand skills, speech, and mobility

Characteristics:
-Deceleration of head growth (starting at 2-4 months of age) leading to microcephaly
-Hypotonia
-Breathing irregularities
-Seizures
-Growth failure
-Intellectual disability
-Scoliosis

Medical management:
-No cure
-Symptomatic and supportive measures
-Surgical spinal fusion for early onset severe scoliosis reduces the risk of severe respiratory infection and increases life expectancy
-Maximize patient’s functional abilities
-Music as a motivational strategy

Prader-Willi syndrome (structural abnormality)Is a rare genetic disorder caused by the loss of function/deletion of chro...
03/28/2026

Prader-Willi syndrome (structural abnormality)

Is a rare genetic disorder caused by the loss of function/deletion of chromosome 15 resulting in severe hypotonia (floppiness), feeding difficulties, and failure to thrive in infancy.

Characteristics:
Almond-shaped eyes
Triangular mouth
Small hands and feet
Lesions in hypothalamus and parasympathetic NS leading to
Daytime sleepiness
Sleep apnea

Thermoregulation disorders

Satiety disorders-constant hunger (hyperphagia) leading to severe obesity

Growth hormone deficiency
osteoporosis
impaired bone growth
short stature
muscle weakness and hypotonia

Orthopedic problems
scoliosis
kyphosis
excessive foot pronation

Behavior problems

Cognitive delays

Spinal muscular atrophy SMA (autosomal recessive)Type 0-Most severeRespiratory support necessary at or shortly after bir...
03/27/2026

Spinal muscular atrophy SMA (autosomal recessive)

Type 0-Most severe
Respiratory support necessary at or shortly after birth
Death within weeks

Type 1-Most common type
Onset age: 0-6 months
Rapidly progressive
Severe hypotonia
Unable to sit
Death at age

Cystic fibrosis "CF" (autosomal recessive)Is a chronic, inherited genetic disorder causing the body to produce thick, st...
03/26/2026

Cystic fibrosis "CF" (autosomal recessive)

Is a chronic, inherited genetic disorder causing the body to produce thick, sticky mucus that clogs lungs, damages the pancreas, and triggers severe digestive issues. It is caused by mutations in the CFTR gene, usually inherited from both parents.

Characteristics:
Respiratory symptoms-mucus (sputum), Wheezing, Exercise intolerance, Repeated lung infections, Inflamed nasal passages or a stuffy nose, Recurrent sinusitis, nasal polyps, hemoptysis, pneumothorax,

Digestive symptoms-Foul-smelling, greasy stools, Poor weight gain and growth, Intestinal blockage, particularly in newborns (meconium ileus), Chronic or severe constipation, which may include frequent straining while trying to pass stool, eventually causing part of the re**um to protrude outside the a**s (re**al prolapse), diabetes, liver disease, intestinal obstruction, distal intestinal obstruction syndrome (DIOS)

Reduced fertility
Osteoporosis
Electrolyte imbalance

Medical management:
Airway clearance techniques

Vest therapy
Oxygen therapy
Ventilation
Feeding tube
Lung transplant
Liver transplant

Antibiotics
Anti-inflammatory medications
Saline
Bronchodilators
Acid reducing medications
Stool softeners

Myotonic dystrophy type 1 (single gene autosomal dominant)Disorder caused by unstable CTG (cytosine-thymine-guanine) tri...
03/25/2026

Myotonic dystrophy type 1 (single gene autosomal dominant)

Disorder caused by unstable CTG (cytosine-thymine-guanine) trinucleotide repeat in the DMPK gene on chromosome 19q13.3. which results in progressive muscle weakness, wasting, and myotonia (delayed relaxation).

Characteristics:
Congenital-Severe hypotonia, muscle weakness, respiratory difficulties

Childhood onset – diagnosed between 1 and 10 years of age
Muscle weakness, including respiratory musculature, Sleep problems, GI disorders, Cognitive and psychiatric problems

Management.
Treatment of manifestations: Use of ankle-foot orthoses, wheelchairs, or other assistive devices; special education support for affected children; treatment of hypothyroidism; management of pain; consultation with a cardiologist for symptoms or EKG evidence of arrhythmia; removal of cataracts if vision is impaired; hormone replacement therapy for males with hypogonadism; surgical excision of pilomatrixoma and basal cell carcinomas.

Prevention of secondary complications: Choice of induction agents, airway care, local anesthesia, and neuromuscular blockade to minimize complications during surgery; cardiac pacemakers or implantable cardioverter-defibrillators may prevent life-threatening arrhythmias; continue physical activity and maintain appropriate weight.

Achondroplasia (single gene autosomal dominant)Is the most common form of short-limbed dwarfism, caused by genetic mutat...
03/25/2026

Achondroplasia (single gene autosomal dominant)

Is the most common form of short-limbed dwarfism, caused by genetic mutation in the FGFR3 gene that inhibits bone growth by disruption of endochondral ossification at epiphyseal plate.

Characteristics:
-Short stature
-Short humerus and femur bilaterally
-Normal trunk size and short extremities
-Macrocephaly
-Kyphosis, kyphoscoliosis
-Sleep apnea

Wolf-Hirschhorn syndrome (structural abnormality)Is a rare genetic disorder caused by partial deletion of the short arm ...
03/23/2026

Wolf-Hirschhorn syndrome (structural abnormality)

Is a rare genetic disorder caused by partial deletion of the short arm in chromosome 4.
Affecting males > females with ratio of 1:2

Characteristics:
-Hypotonia
-Microcephaly
-Intellectual disability
-Wide-spaced eyes (hypertelorism)
-Broad or beaked nose
-Low-set ears with small holes or skin tags
-Delayed growth and development
-Heart defects
-Seizures
-GI organ malformation
-Hearing problems
-Cleft palate/lip

Medical management:
-Medication for seizures/cardiac issues
-G tube or GJ tube for feeding issues

Turner syndrome (numerical abnormality)Is a genetic condition affecting only females caused by the absence of one X chro...
03/22/2026

Turner syndrome (numerical abnormality)

Is a genetic condition affecting only females caused by the absence of one X chromosome in the 23rd pair.

Characteristics include:
-Webbed neck
-Small stature
-Broad chest
-Underdeveloped secondary sexual characteristics
-Hearing impairment
-Bone, kidney and heart abnormalities
-Thyroid problems
-Normal intelligence
-May have learning problems

Medical management:
-Human growth hormone
-Estrogen therapy

Complications:
If left untreated, complications can include high blood pressure, type 2 diabetes, thyroid issues, osteoporosis (due to low estrogen), and heart defects.

It's World Down syndrome Day. ROCK MISMATCHED SOCKS DAY-as the karyotype for Down syndrome looks like mismatched socks. ...
03/21/2026

It's World Down syndrome Day.

ROCK MISMATCHED SOCKS DAY-as the karyotype for Down syndrome looks like mismatched socks.

Down syndrome (numerical abnormality) caused by a third partial or complete copy of 21st chromosome.

Common signs and symptoms include:
Flat hypoplastic face with short nose
Eyes that slope upward at the lateral corners
Epicanthic skin folds – vertical folds of skin extending from the root of the nose to the medial end of the eyebrow
Large, often protruding tongue
Flattened back of the head (brachycephaly)
Small-rounded ears
Broad, small hands and feet
Short toes, with a wide space between the first and second toes
Transverse (simian) palmar crease
Intellectual disability (most common cause in children)
Motor incoordination and decreased motor planning ability
Learning difficulties leading to learning disabilities
Neurological issues-seizures, attention deficits, difficult processing information
Generalized hypotonia
Visual problems-cataracts, myopia, farsightedness, strabismus, nystagmus
Hearing impairments
Heart defects-VSD, ASD
Sleep apnea-tracheomalacia
Lung problems-restrictive pulmonary disease
Thyroid disease
Ligamentous laxity-AA instability- Areflexia, positive Babinski (after ~18 months of age), clonus, changes in gait, headaches, Achilles tendon tightness, increased muscle tone, neck pain, neurogenic bladder, sensory changes, torticollis, vertigo, increased muscle weakness, pes pla**s, calcaneal valgus, patellar instability, hip subluxation, scoliosis

Happy Spring!!RainFlowersTree PollenGet ready to fight seasonal allergies!
03/20/2026

Happy Spring!!

Rain
Flowers
Tree Pollen

Get ready to fight seasonal allergies!

Medical Management for Spina BifidaSurgical closure of the lesion-if caught early enough can be performed in uteroAntico...
03/19/2026

Medical Management for Spina Bifida

Surgical closure of the lesion-if caught early enough can be performed in utero
Anticonvulsant drugs
Diuretic drugs to temporarily decrease CSF volume
Antibiotics for infection control
Re**al suppositories for bowel management
Supplementary calcium to reduce osteoporosis

Neurosurgery
VP-shunt insertion-telescopic with growth, behind the ear
VP-shunt revision
Tethered cord release
Surgery for hydromyelia to restore normal CSF flow

Orthopedic surgeries
Hip relocation
Ankle/foot surgeries to achieve plantigrade position
Derotative osteotomies (femoral or tibial)
Tendon releases
Muscle lengthening
Spinal fusion

Urinary tract surgeries

Symptoms of Spina BifidaMuscle tone varies from flaccid to spastic-Lower motor neuron lesions-flaccid paralysis-Upper mo...
03/18/2026

Symptoms of Spina Bifida

Muscle tone varies from flaccid to spastic
-Lower motor neuron lesions-flaccid paralysis
-Upper motor neuron signs-related to CNS involvement (spasticity and abnormal reflexes)

Sensory deficits-Frequently do not correlate with motor levels
Temperature-Burns
Pressure-skin breakdown

Musculoskeletal deformities
-Spinal deformities-scoliosis, Kyphosis,excessive L-spine lordosis
-Postural problems-anterior pelvic tilt, forward head, rounded shoulders, crouched standing posture
-LE deformities-torsional deformities of femur and tibia (femoral anteversion, external tibial torsion, internal tibial torsion), Hip dysplasia, Hip subluxation, Hip dislocation, Genu varum or valgus, Talipes equinovarus-clubfoot, Calcaneovalgus much more common in a lower level lesion due to gastroc being knocked out and anterior tib still active so causes dorsiflexion contracture, pronated or supinated forefoot
-Joint contractures-Hip flexors, hip abductors and external rotators, knee flexors, ankle dorsiflexors or plantarflexors
Osteoporosis

Hydrocephalus
***Shunt malfunction-irritability, headaches, vomiting, lethargy, fever, speech changes, decreased activity level, decreased school performance, personality change, visual disturbances, change in visual acuity, seizure activity, coordination, muscle tone, appetite***

Arnold-Chiari II malformation- Cerebellar hypoplasia with caudal displacement of the hindbrain through foramen magnum

Seizures

Neurogenic bowel/bladder

Latex allergy

Tethered cord syndrome- onset or worsening of spasticity, sudden increase in lumbar lordosis, back or buttock pain, development or rapid progression of scoliosis, loss of sensation, loss of muscle strength, progressive LE weakness, change in gait pattern, change in bowel and bladder control

Address

Montgomery, TX
77356

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