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3- Metabolic Clinic    

A short glimpse:

Toward the end of the year 1999, it became apparent that an increasing number of patients with inborn errors of metabolism were already following up in the Sunday clinic of general Ward 2, and had been for years, under the care of Dr Dina G Ramadan. These patients were cases either diagnosed in the ward/hospital or referred from other hospitals.

With the growing numbers of referrals of children with metabolic disorders, it was decided that a separate clinic serving these patients was needed and, hence, the establishment of the 'Metabolic Clinic' as a division of the Endocrine Unit.

Patients are referred either for evaluation of a probable metabolic disorder or for follow-up and further management after being diagnosed with an inborn error of metabolism. Currently, the number of files in the clinic exceeds 130 files, with a growing number of about 8 new patients per month. 

The Metabolic Clinic:
 

 1. Run by: Dr Dina G Ramadan , Dr. Ibrahim EL Sharkawy

   2. Clinic Day: Monday

   3. Time:  from 8 am till 12 noon.

New patients come at 8am. Those coming for follow-up are asked not to arrive later than 11:30 to allow time for possible lab testing and to visit the dietitian.

   4. Total accepted new cases: max 3 per day  (by appointment)

   5. Total follow-up: max 10 patients per follow-up day (per appointment).

·        Referrals are accepted from hospitals all over Kuwait, preferably after a phone call. All patients must come with a referring letter and a summary report.

Patient Admission:

  • Patients who are under follow-up and who are ill, have access to their treating doctor any day and to Ward 2 doctors (morning time) and Sabah Hospital Emergency Department at any time.
  • Admission of metabolic patients is to Ward 2

Important Key Personnel:

The care of patients with metabolic problems in Sabah Hospital would never have been successful without the teamwork of the following key persons:

 1. Dr Dina G. Ramadan, Consultant Pediatrician. (Endocrine Unit and Ward 2).2. Dr. Ibrahim EL Sharkawy , paed. specialist

       3- Metabolic Clinic nurses: Sister Enaam, Sister Zainab and Sister Fatma who are   experienced with properly performing the various metabolic tests and sample collection.

      3. Dietitians: particularly Mrs Kulwant.

      4. Ward 2 staff, particularly Dr Amira.  Dr Hassan and Ward 2 nurses who have gained experience in managing the patients during their acute illness.

We appreciate the support of:

     Pediatric Intensive Care Unit (PICU)

     Biochemistry and Hormone lab (Dr Rao and Dr Girish)

Tel  : -- 4812000 - -ext -- 6107

psychiatric Clinic   

Dr / Maghrabi Moh. Maghrabi

Diploma in Medicine. Diploma in  Psychatry ( U.K) .

Dr /Maghrabi attends our hospital from Psychatric Hospital .

Cases seen in the clinic are :

-         Nocturnal enuresis.

-         Encopresis .

-         ADHD .

-         Autism

-         Conduct Disorders

-         Sleep  Disorders

-         Feeding Disorders

-         Conversion and Dissociative Disorders

-         Depressive Disorders

-         Psychotic Disorders

-         Speech Disorders

Tel  :  4815000 – ext 6104 .
 

7-Genetic Clinic :

The Genetic Clinic at Sabah Ped Hospital started at 1978. It is run on Sunday
by Senior Registrar in clinical genetics. It covers areas belonging to Sabah and
Mubarak hospitals areas. It covers all genetic cases including mental retardation
, dysmorphic features as part of a syndrome, short stature, congenital malformations , familial deafness and blindness, childhood autism , premarital
counseling , gynecological cases like repeated pregnancy loss ( abortions ) ,
fetal deaths and infertility . It also includes familial hematological disorders and
familial cancer particularly breast cancer and leukemia.
Facilities for investigations available :
1- Chromosomal  study (karyotype) .  
2- Molecular cytogenetic study ( FISH  technique) :-
    - Detailed study for chromosomal anomalies.
    - Prader - Willi syndrome.
    - Angelman syndrome  .
    - Di George syndrome .
    - William syndrome.
3- Molecular lab ( DNA  analysis ) :
    - Fragile X syndrome .
    - Spinal Muscular Atrophy .
    - Metachromatic  leukodystrophy .
    - Prader - Willi / Angelman syndrome .
    - Myotonic dystrophy.
    - Huntington  chorea.
    - Phenyl ketonuria .
    - Batten disease .
    - Kennedy disease .
    - Autosomal recessive sensor neural hearing loss .
    -  Chloride loosing diarrhea . ( CLD)
    - Testicular feminization syndrome .
    - Sex determination.
    - Noorie disease .
    - Breast cancer .
    - Von Hipple Lindo disease ( VHL ) .
    - Retinoblastoma .
    - Non - Polyposis colon cancer

Average numbers seen / month - 24 patients

Tel : -- 6222
 

 

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