QUIZ 2: CHAPTER 27: NURSING CARE OF THE CHILD BORN WITH A PHYSICAL OR DEVELOPMENTAL CHALLENGE Flashcards

1
Q

Also known as “tongue tied”. The abnormal restriction of tongue by abnormally tight frenulum.
The only management is surgery

A

ANKYLOGLOSSIA

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2
Q

It is a failure of the maxillary & median nasal processes to fuse that range from small notch in the upper lip to total separation of lip & facial structure up into floor of the nose, with even upper teeth and gingiva absent.

A

CLEFT LIP

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3
Q

It is a palate opening that usually on the midline & involves anterior hard palate, posterior soft palate, bath.

A

CLEFT PALATE

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4
Q

is a triad of micrognathia (small mandible), cleft palate, and glossoptosis (a tongue malpositioned downward)

A

PIERRE ROBIN SYNDROME

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5
Q

orifice/passage in body that is closed or absent

A

ATRESIA

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6
Q

abnormal/ surgically made passage between hollow or tubular organ & body surface, between 2 hollow or tubular organs

A

FISTULA

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7
Q

obstruction of esophagus

A

ESOPHAGEAL ATRESIA

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8
Q

connected distally to the trachea is the most common kind af esophageal malformation (classified as Gross type C)

A

ESOPHAGEAL ATRESIA WITH FISTULA

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9
Q

Abdominal contents protruding through wall of abdomen at the junction of UC and abdomen. Intestines are usually herniated but sometimes it Included stomach and liver.

A

Omphalocele

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10
Q

For this condition, anticipate the pt had hydramnios throughout pregnancy.
The findings for newborn is < 30mL gastric contents can be aspirated, distended abdomen and tender to palpate.

A

STENOSIS NARROWING

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11
Q

Anal stricture is narrowing the end af tube that takes stool aut of the body
The other term is “anal stenosis”

A

IMPERFORATE ANUS

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12
Q

is a protrusion of an abdominal organ (usually the stomach or intestine) through a defect in the diaphragm into the chest cavity. This usually occurs on the left side, causing cardiac displacement to the right side of the chest and collapse of the left lung.

A

diaphragmatic hernia

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13
Q

An ___ is a protrusion of a portion of the intestine through the umbilical ring, muscle, and fascia surrounding the umbilical cord

A

umbilical hernia

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14
Q

an excess of CSF in the ventrides or the subarachnaid space
If the fluid can reach the spinal cord, it can be communicating hydrocephalus or extra ventricular hydrocephalus.

A

HYDROCEPHALUS

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15
Q

This happens when the fusion of posterior laminae of vertebrae fails.
Poor pertusian is noticeable when dimpling, abnormal tufts: of hair or any discoloration of skin

A

NEURAL TUBE DISORDERS

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16
Q

is a benign disorder that does not need immediate intervention

A

Spina bifida occulta

17
Q

is when the meninges herniate through unformed vertebrae.
Protruding mass appears and usually have same size of an orange at the center of back.
Layer of skin or just clear dura mater covers the protrusion

A

MENINGOCELE

18
Q

spinal cord & meninges protruding the vertebrae same with meningocele.

A

MYELOMENINGOCELE

19
Q

is a cranial meningocele ar myelomeningacele.
The disorder occurs most often in the occipital area of the skull but may occur as a nasal or nasopharyngeal disorder.

A

ENCEPHALOCELE

20
Q

the absence of cerebral hemispheres. The mother may experience difficulty in labor, mast of this condition present as breech.
If the medulla is intact, the infant may survive several days but without It, the patient cannot survive longer.

A

ANENCEPHALY

21
Q

is a Slow growth of brain that falls more than 3x below normal on growth charts.
This can be caused by infection, severe malnutrition or anoxia in early infancy.

A

MICROCEPHALY

22
Q

Hip Underdevelopment or imperfect hip can affect the head, acetabulum, or both.
The femur head don’t lie deep enough within acetabulum & slips out in movement.
This occurs in females seven times more often than males

A

DEVELOPMENTAL HIP DYSPLASIA

23
Q
  • mildest form; femoral head remains in acetabulum.
A

Acetabular dysplasia

24
Q
  • most common form; femoral head partially displaced.
A

Subluxation

25
Q
  • femoral head not in contact with acetabulum; displaced posteriorly and superiorly
A

Dislocation

26
Q

This condition can result from ingestion of maternal drug, viral invasion, and amniotic band formation.
Prostheses of lower extremity are fitted as early as 6 months while upper extremity are fitted this early so infant can handle and explore objects readily.

A

ABSENT OR MALFORMED EXTREMITIES

27
Q

is a presence of one or additional fingers or toes.

A

POLYDACTYLY

28
Q

is when two fingers or toes are fuse

A

SYNDACTYLY

29
Q

[separation of digits can be done]

A

Webbing

30
Q

[cannot be fully reconstructed]

A

Bones are fused

31
Q

is the indentation of the lower poortion of the sternum. There can be decreased lung volume, and the heart is displaced to the left.

A

PECTUS EXCAVATUM

32
Q

is when the sternum is displaced anteriorly, increasing AP diameter of the chest

A

PECTUS CARINATUM

33
Q

a term derived from tortus (twisted) and callum (neck)-Torticollis (wry neck) accurs as a congenital anomaly when the sternacleidomastaid muscle is injured and bleeds during birth

A

TORTICOLLIS (WRY NECK)

34
Q

The sutures of the skull is closing prematurely and may occur in utero or early infancy
This condition needs to be detected early because sealed skull will compromise brain growth.

A

CRANIOSYNOSTOSIS

35
Q

Achondroplasia(chondrodystrophia) is a failure of bone growth inherited as a dominant trait.
It causes a disorder in cartilage production in utero.
The epiphyseal plate of long bones cannot produce adequate cartilage for longitudinal bone growth, which results in both arms and legs becoming stunted.

A

ACHONDROPLASIA

36
Q

is a word formed from the Latin words talus (“ankle”) and pes (“foot”)
The __ deformities are ankle-foot disorders, popularly called clubfoot
With the orthopedic correction techniques currently available, correction should leave the child with normal foot position.

A

Talipes