84 Citations
Floppy Baby Syndrome: A Comprehensive Review of the Chromosomal Abnormalities and Gene Mutations
- Medicine
- 2020
In the process of evaluating floppy infant syndrome and attempting to narrow down to the primary cause of floppy infant Syndrome (FIS), it is imperative to determine whether the cause of FIS is peripheral or central.
Genetic evaluation of the floppy infant.
- Medicine, BiologySeminars in fetal & neonatal medicine
- 2011
Evaluation of children with peripheral hypotonia by electroneuromyography
- Medicine, Psychology
- 2016
The most common neuromuscular disorder was peripheral neuropathy, whereas the least common cause was neurmuscular junction disorder in a sample of Egyptian children.
Hypotonia and Lethargy in a Two-Day-Old Male Infant
- MedicinePediatrics
- 2019
An expert panel discusses the differential diagnosis of hypotonia in a neonate, offers diagnostic and management recommendations, and discusses the final diagnosis.
Neonatal hypertonia: I. Classification and structural-functional correlates.
- Medicine, PsychologyPediatric neurology
- 2008
Clinical Reasoning: A tale of a hypotonic infant
- MedicineNeurology
- 2016
An 11-month-old girl was referred to the authors' center for evaluation of hypotonia and developmental delays because of breech presentation and had significant swallowing dysfunction requiring nasogastric tube feeding.
A Pilot Study for Evaluation of Hypotonia in Children With Neurofibromatosis Type 1
- MedicineJournal of child neurology
- 2015
Multivariate logistic regression analysis showed the presence of head lag on a pull-to-sit test paired with increased hip range of motion is an accurate predictor of hypotonia in children with neurofibromatosis type 1.
References
SHOWING 1-10 OF 32 REFERENCES
Hypotonia, Congenital Hearing Loss, and Hypoactive Labyrinths
- Medicine, PsychologyJournal of child neurology
- 2003
Four patients attending a neurosensory genetics clinic over an 11-year period presented with sensorineural hearing loss, hypotonia, and delay in the acquisition of motor milestones, demonstrating that hypoactive labyrinthine function may be associated with hypotonia that is severe enough to result in delayed acquisition ofMotor milestones.
Macrocerebellum: Neuroimaging and Clinical Features of a Newly Recognized Condition
- Psychology, MedicineJournal of child neurology
- 1997
It is proposed that the cerebellum is responding to the elaboration of growth factors intended to augment the slow development of cerebral structures and probably represents a marker for disturbed cerebral development.
The floppy infant.
- MedicineAmerican journal of diseases of children
- 1961
Investigations have proved that the pathology of many cases of "amyotonia congenita" is the same as that of Werdnig-Hoffmann's disease, namely a degeneration of anterior horn cells of the spinal cord.
Hypoactive Labyrinths and Motor Development
- MedicineClinical pediatrics
- 1974
Counseling of parents of deaf children who walk late should be delayed until vestibular testing has been carried out to avoid false diagnoses of associated brain damage or mental retardation.
Treatment of spastic gait in cerebral palsy.
- Medicine, PsychologyThe West Virginia medical journal
- 1994
In a series of operations in 19 children with spastic diplegia, a procedure in which there is selective section of portions of the dorsal roots L2-S2 was able to decrease their spasticity significantly with resultant improvement in motor function and self care.
Congenital muscular dystrophy associated with calf hypertrophy, microcephaly and severe mental retardation in three Italian families: evidence for a novel CMD syndrome
- MedicineNeuromuscular Disorders
- 2000
The congenital muscular dystrophies in 2004: a century of exciting progress
- MedicineNeuromuscular Disorders
- 2004
The congenital and limb-girdle muscular dystrophies: sharpening the focus, blurring the boundaries.
- Medicine, BiologyArchives of neurology
- 2004
The different groups of proteins currently recognized as being involved in congenital and limb-girdle muscular dystrophies are reviewed, associated them with the clinical phenotypes, and some clinical and molecular clues that are helpful in the diagnostic approach to these patients are determined.
126th International Workshop: Congenital Myasthenic Syndromes, 24–26 September 2004, Naarden, The Netherlands
- Biology, MedicineNeuromuscular Disorders
- 2005
Evolution of nerve conduction abnormalities in children with dominant hypertrophic neuropathy of the charcot‐marie‐tooth type
- Medicine, PsychologyMuscle & nerve
- 1983
Serial motor conduction velocities and distal motor latencies were determined in two pairs of dizygotic twins born to a parent with dominant hypertrophic neuropathy of the Charcot‐Marie‐Tooth type (HMSN‐I) and showed that maximal slowing of motor nerve conduction Velocities evolved over the first 3–5 years of life in HMSN‐ I.