Dr. KANTA HALDER
Resident (MD;Phase A)
BICH
Particulars of the patient
 Name: Omar Ali.
 Age: 1 year 6 months.
 Sex: Male.
 Address: Purbososhalia, Noakhali.
 Date of Admission: 28.11.2015.
 Date of Examination: 06.12.2015.
Chief Complaints
 Repeated seizure since 2 months of
age.
 No neck control till date.
History of present illness
According to the statement of mother, her
child was suffering from repeated seizure since
2 months of age which was generalized tonic in
nature, persisted for 5 to 10 minutes and
occurred for about 8 to 10 times in a day.
Mother also noticed that her child did not
have neck control yet, developed stiffness of
all limbs and had feeding difficulty since early
infancy.
History of present illness(cont..)
He had no history of head trauma or CNS
infection. With these complaints, they consulted
a local physician who advised some medications
and referred the child to Dhaka Shishu Hospital
for further evaluation and better management.
History of Past illness
He was admitted to Dhaka Shishu Hospital 2
months back due to acute watery diarrhoea.
Birth History
Antenatal : Mother, Rehana Akter was on
irregular antenatal check up. She had no history
of HTN, GDM, fever with rash or taking any
offending drug during her pregnancy period.
Natal : Baby was born by vaginal delivery at
term at home with average birth weight. There
was h/o maternal prolong labour with prolong
rupture of membrane for 2 days.
Birth History (cont..)
Postnatal : Baby did not cry after birth, admitted
to a local hospital and developed seizure at 2
hours of age. He was discharged at 7 days of age
after control of seizure. There was no history of
neonatal jaundice.
Feeding History
Baby was on exclusive breast feeding up to 4
months of age, then formula feeding was
started along with suji.
Immunization History
He is immunized as per EPI schedule.
Family History
He is the only issue of his non-consanguineous
parents.
Socio-economic History
He came from a low socio-economic family.
Treatment History
He was treated with oral phenobarbitone with
adequate dose for about last 4 – 5 months.
After admission, he also got some other
medications along with phenobarbitone.
Developmental Milestone
• No neck control yet.
• No social smile or interaction.
• No babbling, crying sound only.
General Examination :
Appearance: Ill looking, not interested to
surrounding, no facial dysmorphysm.
Anaemia: Mildly pale.
Jaundice:
Cyanosis:
Clubbing: Absent.
Oedema:
Dehydration:
Cont..
Skin: BCG mark present, no neurocutaneous
stigmata.
Lymphnode: Not palpable.
Signs of meningeal irritation: Absent.
Ear:
Nose: Normal.
Throat:
Cont..
Vital Signs:
Heart Rate: 100/min
Respiratory Rate: 32/min
Temperature: 99°F
Blood Pressure: 90/50 mmHg
Cont..
Anthropometry:
OFC: 41 cm (microcephaly).
Weight: 7.1 kg.
Height: 68 cm.
HAZ: -4.6 SD (severely stunted).
WHZ: - 1.40 SD (normal).
Nervous System Examination
 Higher psychic Function :
Conscious, not oriented to surroundings.
 Cranial nerves examination :
No facial dysmorphysm.
Pupillary size and shape was normal, light
reflex was present.
No squint, eye balls moved in all direction.
Drooling was present, swallowing difficulty
was present.
Cont..
 Motor function :
Muscle bulk : Reduced in all 4 limbs.
Muscle tone : Increased in all 4 limbs, more in
upper limbs.
Muscle power : 2/5 in all 4 limbs.
Reflexes : Normal in all 4 limbs.
Clonus : Absent.
Planter response : Bilaterally extensor.
Involuntary movement : Absent.
 Sensory function : Seems to be intact.
 Fundoscopy : Normal.
Developmental Assessment
 Gross motor :
Pulled to sit - Head lags behind the body line.
 Fine motor :
Couldn’t reach and hold object.
No midline activity.
 Cognition :
Recognizes mother’s lap.
No social smile.
Cont..
 Vision :
Fixes and follows coloured object.
 Hearing :
Doesn’t turn to rattling sound.
 Speech :
No babbling, crying only.
Other systemic examination including
Abdominal examination revealed normal
findings.
Salient feature
Omar Ali, 1 year 6 months old male child, only
issue of his non-consanguineous parents, was
admitted with the complaints of generalized
tonic seizures since 2 months of age, stiffness
of limbs which was more in upper limbs and
no neck control with swallowing difficulty
since early infancy. He had definite history of
perinatal asphyxia with seizure, but no history
of neonatal jaundice, low birth weight or any
significant maternal illness during pregnancy.
Cont..
Omar was mildly pale, severely stunted,
having microcephaly, no neurocuteneous
stigmata or organomegaly. Vitals were within
normal limit. His cranial nerves were intact
except swallowing difficulty , muscle bulk &
power was reduced, but tone was increased in
all limbs (more in upper limbs); motor,
cognition and speech delay was present with
impaired vision and hearing.
Provisional Diagnosis
Spastic tetraplegic cerebral palsy with
microcephaly with epilepsy with motor,
cognition and speech delay with impaired
vision and hearing with secondary
malnutrition.
Differential Diagnosis
Neurometabolic disease with microcephaly
with epilepsy with motor, cognition and
speech delay with impaired vision and hearing
with secondary malnutrition.
Investigations
Complete Blood Count :
• Hb%: 11.9 gm/dl
• WBC: Total count: 10,900/cumm
Differential count:
o Neutrophil: 43%
o Lymphocyte: 53%
o Monocyte: 02%
o Eosinophil: 02%
o Basophil : 00%
Cont..
o RBC:Normocytic normochromic
o WBC:Mature with above
distribution
o Platelet: Adequate
• Platelet : 3,48,000/cumm
• PBF:
Cont..
RBS : 3.4 mmol/L.
S. Electrolytes : Na⁺ - 141.5 mmol/L.
K⁺ - 4.0 mmol/L.
Cl⁻ - 103.6 mmol/L.
S. Calcium : 2.26 mmol/L.
SGPT : 40 U/L.
Cp omar ali
Cp omar ali
Cont..
CT Scan of Brain : Mildly dilated ventricles
with widened CSF spaces.
EEG : Epileptiform discharge over B/L
temporo-parieto-occipital area.
Final Diagnosis
Spastic tetraplegic cerebral palsy with
microcephaly with epilepsy with motor,
cognition and speech delay with impaired
vision and hearing with secondary
malnutrition.
Management
Multidisciplinary team approach :
Paeditritian/Paediatric neurologist works as a
team leader involving-
• Physiotherapist.
• Occupational therapist.
• Speech-language therapist.
• Psychologist.
• Ophthalmologist.
• ENT specialist.
• Orthopaedic surgeon.
• Special school and teacher & social worker.
Cont..
 Counseling.
 Nutritional management :
NG tube feeding (F - 75).
Multivitamin, folic acid, Vitamin A and zinc
supplementation.
 Management of epilepsy :
Syp Phenobarbitone.
Tab Nitrazepum.
Cont..
 Management of spasticity :
Tab Beclofen.
Physiotherapy.
 For vision & hearing :
Consultation with ophthalmologist and ENT
specialist.
 Neuro-developmental therapy and
stimulation.
 Follow up
THANK YOU

More Related Content

PPTX
cerebral palsy - case presentation ^.pptx
PPTX
OSCE APRIL 2022-PART-3 -PAED.pptx
PPT
Case Study - Cerebral Palsy
PPTX
A Case of Amyotrophic Lateral Sclerosis
PPT
Case presentation- A Pediatric Neurological case..!!
PPTX
Cerebral palsy case presentation
PPTX
Muscle tone munish G B PANT DELHI
PPT
5. PDA
cerebral palsy - case presentation ^.pptx
OSCE APRIL 2022-PART-3 -PAED.pptx
Case Study - Cerebral Palsy
A Case of Amyotrophic Lateral Sclerosis
Case presentation- A Pediatric Neurological case..!!
Cerebral palsy case presentation
Muscle tone munish G B PANT DELHI
5. PDA

Viewers also liked (20)

PPTX
Thalassemia.final
PPTX
Itp.kanta
PPTX
N sepsis
PPTX
Sumaiya, irns
PPTX
Ptvlbw with n jaundice
PPTX
PPTX
Rh incompatibility
PPTX
Congenital ns
PPTX
Lung agenesis
PPTX
Shifa collapse consolidation
PPTX
Pna mas
PPTX
Sdns with toxicity
PPTX
Cp sushmita
PPTX
Sam , 6 mo
PPTX
Viral hep a
PPTX
Empyema.
PPTX
Rta 18.05.16
PPTX
Agn with hf
PPTX
Abo incompatibility
PPTX
All...rim
Thalassemia.final
Itp.kanta
N sepsis
Sumaiya, irns
Ptvlbw with n jaundice
Rh incompatibility
Congenital ns
Lung agenesis
Shifa collapse consolidation
Pna mas
Sdns with toxicity
Cp sushmita
Sam , 6 mo
Viral hep a
Empyema.
Rta 18.05.16
Agn with hf
Abo incompatibility
All...rim
Ad

Similar to Cp omar ali (20)

PPTX
CP BY AKHI.pptx
PPTX
West syndrome
PPTX
PPTX
Henoch–Schönlein purpura
PPTX
chronic liver disease
PPTX
PPT ON GBS BASIC PRESENTATION WITH RELAVANT INFORMATION
PPTX
Spastic quadriplegia with motor, cognition delay with vision and hearing imp...
PPTX
West syndrome case presentation
PPTX
Long case on hypoparathyroidism bya dr.hasan al banna
PPTX
EPILEPSY FINAL.pptxEpilepsy is common. It's estimated that 1.2% of people in ...
PPTX
Tuberous Sclerosis
PPTX
Whiteout disease
PPTX
A case presentation on cerebrovascular accident.pptx
PPTX
stroke CVaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaA.pptx
PPTX
10. asthma
PPTX
10. asthma
PPTX
A 22 yr old male with forgetfullness.pptx
PPTX
Acute Leukemia
PPTX
Bronchiolitis -case presentation
PPTX
Juvenile Colonic Polyp
CP BY AKHI.pptx
West syndrome
Henoch–Schönlein purpura
chronic liver disease
PPT ON GBS BASIC PRESENTATION WITH RELAVANT INFORMATION
Spastic quadriplegia with motor, cognition delay with vision and hearing imp...
West syndrome case presentation
Long case on hypoparathyroidism bya dr.hasan al banna
EPILEPSY FINAL.pptxEpilepsy is common. It's estimated that 1.2% of people in ...
Tuberous Sclerosis
Whiteout disease
A case presentation on cerebrovascular accident.pptx
stroke CVaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaA.pptx
10. asthma
10. asthma
A 22 yr old male with forgetfullness.pptx
Acute Leukemia
Bronchiolitis -case presentation
Juvenile Colonic Polyp
Ad

Recently uploaded (20)

PPTX
Method of organizing health promotion and education and counselling activitie...
PPTX
Journal Article Review - Ankolysing Spondylitis - Dr Manasa.pptx
PPT
intrduction to nephrologDDDDDDDDDy lec1.ppt
PPTX
PRE ECLAPSIA AND ECLAPSIA presentation-1.pptx
PPTX
ARTHRITIS and Types,causes,pathophysiology,clinicalanifestations,diagnostic e...
PPTX
Critical Issues in Periodontal Research- An overview
PPTX
Local Anesthesia Local Anesthesia Local Anesthesia
PDF
495958952-Techno-Obstetric-sminiOSCE.pdf
PPTX
المحاضرة الثالثة Urosurgery (Inflammation).pptx
PDF
periodontaldiseasesandtreatments-200626195738.pdf
PPTX
Hypertensive disorders in pregnancy.pptx
PPTX
presentation on dengue and its management
PPTX
SUMMARY OF EAR, NOSE AND THROAT DISORDERS INCLUDING DEFINITION, CAUSES, CLINI...
PDF
Geriatrics Chapter 1 powerpoint for PA-S
PPTX
01. cell injury-2018_11_19 -student copy.pptx
PDF
Diabetes mellitus - AMBOSS.pdf
PPTX
etomidate and ketamine action mechanism.pptx
PDF
neonatology-for-nurses.pdfggghjjkkkkkkjhhg
PPTX
Biostatistics Lecture Notes_Dadason.pptx
PPTX
Peripheral Arterial Diseases PAD-WPS Office.pptx
Method of organizing health promotion and education and counselling activitie...
Journal Article Review - Ankolysing Spondylitis - Dr Manasa.pptx
intrduction to nephrologDDDDDDDDDy lec1.ppt
PRE ECLAPSIA AND ECLAPSIA presentation-1.pptx
ARTHRITIS and Types,causes,pathophysiology,clinicalanifestations,diagnostic e...
Critical Issues in Periodontal Research- An overview
Local Anesthesia Local Anesthesia Local Anesthesia
495958952-Techno-Obstetric-sminiOSCE.pdf
المحاضرة الثالثة Urosurgery (Inflammation).pptx
periodontaldiseasesandtreatments-200626195738.pdf
Hypertensive disorders in pregnancy.pptx
presentation on dengue and its management
SUMMARY OF EAR, NOSE AND THROAT DISORDERS INCLUDING DEFINITION, CAUSES, CLINI...
Geriatrics Chapter 1 powerpoint for PA-S
01. cell injury-2018_11_19 -student copy.pptx
Diabetes mellitus - AMBOSS.pdf
etomidate and ketamine action mechanism.pptx
neonatology-for-nurses.pdfggghjjkkkkkkjhhg
Biostatistics Lecture Notes_Dadason.pptx
Peripheral Arterial Diseases PAD-WPS Office.pptx

Cp omar ali

  • 1. Dr. KANTA HALDER Resident (MD;Phase A) BICH
  • 2. Particulars of the patient  Name: Omar Ali.  Age: 1 year 6 months.  Sex: Male.  Address: Purbososhalia, Noakhali.  Date of Admission: 28.11.2015.  Date of Examination: 06.12.2015.
  • 3. Chief Complaints  Repeated seizure since 2 months of age.  No neck control till date.
  • 4. History of present illness According to the statement of mother, her child was suffering from repeated seizure since 2 months of age which was generalized tonic in nature, persisted for 5 to 10 minutes and occurred for about 8 to 10 times in a day. Mother also noticed that her child did not have neck control yet, developed stiffness of all limbs and had feeding difficulty since early infancy.
  • 5. History of present illness(cont..) He had no history of head trauma or CNS infection. With these complaints, they consulted a local physician who advised some medications and referred the child to Dhaka Shishu Hospital for further evaluation and better management.
  • 6. History of Past illness He was admitted to Dhaka Shishu Hospital 2 months back due to acute watery diarrhoea.
  • 7. Birth History Antenatal : Mother, Rehana Akter was on irregular antenatal check up. She had no history of HTN, GDM, fever with rash or taking any offending drug during her pregnancy period. Natal : Baby was born by vaginal delivery at term at home with average birth weight. There was h/o maternal prolong labour with prolong rupture of membrane for 2 days.
  • 8. Birth History (cont..) Postnatal : Baby did not cry after birth, admitted to a local hospital and developed seizure at 2 hours of age. He was discharged at 7 days of age after control of seizure. There was no history of neonatal jaundice.
  • 9. Feeding History Baby was on exclusive breast feeding up to 4 months of age, then formula feeding was started along with suji. Immunization History He is immunized as per EPI schedule.
  • 10. Family History He is the only issue of his non-consanguineous parents. Socio-economic History He came from a low socio-economic family.
  • 11. Treatment History He was treated with oral phenobarbitone with adequate dose for about last 4 – 5 months. After admission, he also got some other medications along with phenobarbitone.
  • 12. Developmental Milestone • No neck control yet. • No social smile or interaction. • No babbling, crying sound only.
  • 13. General Examination : Appearance: Ill looking, not interested to surrounding, no facial dysmorphysm. Anaemia: Mildly pale. Jaundice: Cyanosis: Clubbing: Absent. Oedema: Dehydration:
  • 14. Cont.. Skin: BCG mark present, no neurocutaneous stigmata. Lymphnode: Not palpable. Signs of meningeal irritation: Absent. Ear: Nose: Normal. Throat:
  • 15. Cont.. Vital Signs: Heart Rate: 100/min Respiratory Rate: 32/min Temperature: 99°F Blood Pressure: 90/50 mmHg
  • 16. Cont.. Anthropometry: OFC: 41 cm (microcephaly). Weight: 7.1 kg. Height: 68 cm. HAZ: -4.6 SD (severely stunted). WHZ: - 1.40 SD (normal).
  • 17. Nervous System Examination  Higher psychic Function : Conscious, not oriented to surroundings.  Cranial nerves examination : No facial dysmorphysm. Pupillary size and shape was normal, light reflex was present. No squint, eye balls moved in all direction. Drooling was present, swallowing difficulty was present.
  • 18. Cont..  Motor function : Muscle bulk : Reduced in all 4 limbs. Muscle tone : Increased in all 4 limbs, more in upper limbs. Muscle power : 2/5 in all 4 limbs. Reflexes : Normal in all 4 limbs. Clonus : Absent. Planter response : Bilaterally extensor. Involuntary movement : Absent.  Sensory function : Seems to be intact.  Fundoscopy : Normal.
  • 19. Developmental Assessment  Gross motor : Pulled to sit - Head lags behind the body line.  Fine motor : Couldn’t reach and hold object. No midline activity.  Cognition : Recognizes mother’s lap. No social smile.
  • 20. Cont..  Vision : Fixes and follows coloured object.  Hearing : Doesn’t turn to rattling sound.  Speech : No babbling, crying only. Other systemic examination including Abdominal examination revealed normal findings.
  • 21. Salient feature Omar Ali, 1 year 6 months old male child, only issue of his non-consanguineous parents, was admitted with the complaints of generalized tonic seizures since 2 months of age, stiffness of limbs which was more in upper limbs and no neck control with swallowing difficulty since early infancy. He had definite history of perinatal asphyxia with seizure, but no history of neonatal jaundice, low birth weight or any significant maternal illness during pregnancy.
  • 22. Cont.. Omar was mildly pale, severely stunted, having microcephaly, no neurocuteneous stigmata or organomegaly. Vitals were within normal limit. His cranial nerves were intact except swallowing difficulty , muscle bulk & power was reduced, but tone was increased in all limbs (more in upper limbs); motor, cognition and speech delay was present with impaired vision and hearing.
  • 23. Provisional Diagnosis Spastic tetraplegic cerebral palsy with microcephaly with epilepsy with motor, cognition and speech delay with impaired vision and hearing with secondary malnutrition.
  • 24. Differential Diagnosis Neurometabolic disease with microcephaly with epilepsy with motor, cognition and speech delay with impaired vision and hearing with secondary malnutrition.
  • 25. Investigations Complete Blood Count : • Hb%: 11.9 gm/dl • WBC: Total count: 10,900/cumm Differential count: o Neutrophil: 43% o Lymphocyte: 53% o Monocyte: 02% o Eosinophil: 02% o Basophil : 00%
  • 26. Cont.. o RBC:Normocytic normochromic o WBC:Mature with above distribution o Platelet: Adequate • Platelet : 3,48,000/cumm • PBF:
  • 27. Cont.. RBS : 3.4 mmol/L. S. Electrolytes : Na⁺ - 141.5 mmol/L. K⁺ - 4.0 mmol/L. Cl⁻ - 103.6 mmol/L. S. Calcium : 2.26 mmol/L. SGPT : 40 U/L.
  • 30. Cont.. CT Scan of Brain : Mildly dilated ventricles with widened CSF spaces. EEG : Epileptiform discharge over B/L temporo-parieto-occipital area.
  • 31. Final Diagnosis Spastic tetraplegic cerebral palsy with microcephaly with epilepsy with motor, cognition and speech delay with impaired vision and hearing with secondary malnutrition.
  • 32. Management Multidisciplinary team approach : Paeditritian/Paediatric neurologist works as a team leader involving- • Physiotherapist. • Occupational therapist. • Speech-language therapist. • Psychologist. • Ophthalmologist. • ENT specialist. • Orthopaedic surgeon. • Special school and teacher & social worker.
  • 33. Cont..  Counseling.  Nutritional management : NG tube feeding (F - 75). Multivitamin, folic acid, Vitamin A and zinc supplementation.  Management of epilepsy : Syp Phenobarbitone. Tab Nitrazepum.
  • 34. Cont..  Management of spasticity : Tab Beclofen. Physiotherapy.  For vision & hearing : Consultation with ophthalmologist and ENT specialist.  Neuro-developmental therapy and stimulation.  Follow up