Specialist in Paediatrics

The centre is staffed by paediatric specialists and medical staff to provide professional medical services for infants and children (including medical consultation, various examinations, vaccination, etc.), where the doctor will give professional diagnosis advice, and customize treatment for children.
At the same time, medical staff will closely escort and follow-up the entire process to ensure that parents and babies are under good care.
We are committed to providing quality medical services, hygienic and a comfortable environment. We are dedicated to guard with your baby's health
and happiness.
We are committed to maintaining a high level of quality of service and a healthy environment to give confidence to parents.

Scope of Services

  • Admission to Private Hospitals and in-patient services
  • In-patient examination and treatment for newborn babies

 

 

 (Conducted by paediatrician)

 

  • 6 in 1 (DTaP-IPV-HibHepB) (Diphtheria, Tetanus, Acellular pertussis, Hepatitis B, Inactivated polio and Haemophilus influenzae type B
    conjugate vaccine)
  • 5 in 1 (DTaP-Hib-IPV) (Diphtheria, Tetanus, Acellular pertussis, Inactivated polio and Haemophilus influenzae type b conjugate vaccine)
  • MMR (Measles, Mumps and Rubella vaccine)
  • MMRV (Measles, Mumps, Rubella and Varicella vaccine)
  • Varicella Vaccine
  • HepA (Hepatitis A vaccine)
  • HepB (Hepatitis B vaccine)
  • MenACWY-135 conj (Meningococcal ACWY-135 conjugate vaccine)
  • Hib (Haemophilus influenzae type b vaccine)
  • Rotarix – Rotavirus vaccine
  • RotaTeq – Rotavirus vaccine
  • PCV13 (Pneumococcal conjugate vaccine (13-valent))
  • JE-CV_LiveAtd (Japanese encephalitis vaccine, live attenuated (Chimeric virus))
  • Influenza vaccine
  • HPV (Human papillomavirus vaccine)

 

* Before every vaccination, the doctor will perform a basic physical examination to determine if babies condition are suitable

for vaccination.

 

 

Metabolic disease is a rare genetic disease. Severe metabolic diseases can be fatal in infants and children. Therefore, it is very important to

diagnose and treat them early. It is recommended that all newborn babies to receive screening within several days after birth.

 

Neonatal metabolic disease can be performed on urine or blood samples collected form babies. Blood tests are recognized as international

standards by most countries. Now only a small amount of blood sample can effectively detect more than 30 metabolic diseases for newborn

babies, including most metabolic diseases (amino acid disorders, fatty acid oxidation disorders, or organic acid disorders) that can be

diagnosed and treated.

 

 

“Allergy” refers to the response of the body’s immune system to alien substances (allergens). Symptoms can occur on anywhere of the body,

including eczema, skin irritation, wheezing, vomiting, watery eyes, and nasal discharge. In severe cases, it can cause anaphylactic shock

reactions or tracheal contractions, impeding breathing, and potentially killing. There are many kinds of allergens, such as dust mites, animal

dander, hair, pollen, peanuts, and seafood, which are all common allergens.

 

* If you find that you have eczema, allergic rhinitis, or a sensitive reaction such as skin irritation or dyspnea after eating, you

should seek medical advice to identify the culprits of allergy.

 

 

Sleep apnea in children is a chronic disease. The main symptoms of the early stage are snaring at night. When suffering from sleep apnea

for a long time, children are affected by the low quality of sleep at night and intermittent hypoxia. In severe cases, it will lead to learning

difficulties, behavioral problems, slow growth, and in long term even cardiovascular diseases such as pulmonary hypertension and heart

failure.

 

To accurately diagnose children with sleep apnea, sleep study is a key investigation. Children of any age can receive a sleep test. The child

needs to stay in hospital for one night. Before going to bed, the test technician will place recording devices on the child’s head and body to

record the child’s brain waves, respiration, electrocardiogram, oxygen saturation and other important data. The sleep test process will not

cause any pain. Sleep test data will be interpreted by a specialist to determine if the child has sleep apnea and its severity.

 

* Children with daytime behavior problems, lack of concentration, and emotional instability are also suggested to visit clinical

psychologists.

 

  • Detailed medical history evaluation
  • Physical examination (height, weight, blood pressure, pulse, body weight index)
  • Vision examination by medical staff
  • Intelligence Development Test
  • Routine urinalysis
  • Fecal Analysis: parasites and occult blood
  • Baby and children blood tests

 

 

When children have hearing problems, they often repeat sentences because they do not understand what people are saying. They may be

mistaken for slow response, lack of attention, or poor perception. Not only does it create obstacles to learning, it can also seriously affect

development. To know if children have hearing problems, parents can keep track of their daily behaviors and reactions.

 

The following are some of the signs that children have weak hearing ability:

  • Difficult to distinguish the source of sound
  • Slow response to softer speech
  • Turn his head to one side when listening
  • Often feel that others speech is unclear
  • Unanswered or misunderstood instructions
  • Easy to confuse vocabularies with similar pronunciation
  • The speaker is often asked to repeat what he says, such as “What did you say?” or “Please say it again!”
  • Like to increase the volume of the TV
  • Misarticulation
  • Earache or tinnitus

 

Newborn babies can receive hearing screening tests. The otoacoustic emission test is performed with a probe tube microphone placed in the

ear canal and then emits a sound. If the auditory cells are normal, an otoacoustic response will occur. If the test finds no response, the infant

will have to undergo further tests.

 

 

The period between zero and eight years is an important stage for children’s visual ability to develop. In the development stage, if there is a

” squint ” or severe congenital binocular vision difference, it can lead to amblyopia. If the golden period of treatment is missed, it could result

in long term vision defects, in severe cases can even lead to blindness. Early detection is important in optioning visual outcome.

 

 

EJ Paediatrics
Suite 1430, 14/F,

Ocean Centre, Harbour City,

5 Canton Road, TST, HK

 

Tel : +852 2396 3335