Pediatrics Flashcards

1
Q

What’s the second most common cause of stridor in neonates?

A

Vocal cord paralysis

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2
Q

Which IGg deficiency associated with susceptibility to encapsulated bacteria

A

IGG2

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3
Q

In adults what is the most common IGg deficiency

A

Igg3 susceptibility to uri, AR and asthma

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4
Q

What are the centor criteria for GABHS in children

A

Fever, tender neck adenopathy, exudative tonsillitis, and absence of cough

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5
Q

What is Melnick Fraser syndrome

A

Branchial-oto-renal

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6
Q

What is the treatment for Kawasaki disease?

A

Ivig and aspirin

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7
Q

Symptoms of Usher Type 1

A

retinitis pigmentosa, profound SNHL from birth, vestibular dysfunction

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8
Q

Symptoms of Usher type 2

A

SNHL in adolescence, NO vestibular dysfunction, no retinitis pigmentosa, most common syndromic form of hearing loss

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9
Q

Usher type 3

A

Similar to 1 but milder symptoms, progressive hearing loss, visual loss at puberty

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10
Q

What is the most common IgG class deficiency in children?

A

IgG2, predisposes to recurrent infections to polysaccharide encapsulated bacteria such as H Flu, strep pneumo, and klebsiella

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11
Q

What is the most common IgG deficiency in adults?

A

IgG3

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12
Q

Branchial groove/cleft corresponds to which embryonic cell derivative?

A

Ectoderm

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13
Q

Branchial arch is what embryonic cell derivative?

A

Mesoderm

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14
Q

Branchial pouch corresponds to which embryonic cell derivative?

A

Endoderm

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15
Q

What are the four types of VPI closure?

A

° Coronal (55 %, most common) ° Sagittal (10–15 %, least common) ° Circular (10–20 %) ° Circular with Passavant’s ridge (15–20 %)

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16
Q

What is prominauris

A

absent antihelical fold, abnormally distal insertion of antitragus muscle, excess conchal bowl

17
Q

What does CATCH-22 stand for in DiGeorge Syndrome?

A

Cardiac defects, Abnormal facies, Thymic hypoplasia, Cleft palate, and Hypocalcaemia resulting from 22q11 deletions.

18
Q

What percentage of parotid neoplasms in children are malignant?

19
Q

What are the most common locations of rhabdomyosarcoma in descending order

A

Orbit Nasopharynx Middle ear/mastoid Sinonasal cavity

20
Q

What syndrome is PAX3 gene mutation associated with?

A

Waardenburg

21
Q

Mnemonic for autosomal dominant syndromes

22
Q

normal anatomy of the ear in pediatrics

A

Normal anatomy: 15- to 30-degree posterior angulation, auriculocephalic angle of 20 to 35 degrees; normal pinna position is 15 to 20 mm from the helical rim to the scalp

23
Q

When are lymphatic malformations diagnosed

A

40% in neonatal period, 60% by age 1, 90% by age 3

24
Q

stain for bartonella?

A

Warthin starry silver stain

25
What is a pilomatrixoma?
Calcifying epitheolioma of malherbe Arises from the outer root sheath sell of hair follicle
26
What is the most common malignancy in infants less than 1 year of age?
Neuroblastoma
27
Is coronary artery aneurysm an early or late symptom of kawasaki disease?
Late
28
During which week of development does the EAC recanalize?
28th week
29
During which week of development do the hillocks of his develop, and then by which week do they fuse to form the auricle?
6th week, 12th week
30
31
What is the likelihood of a negative bronch in the setting of unwitnessed choking episode?
60%
32
What is the blood supply to the adenoid
Pharyngeal branch of the internal maxillary (major supply) Ascending palatine branch of the facial artery Ascending cervical branch of thyrocervical trunk Ascending pharyngeal artery
33
What are the most common sites of rhabdo in descending order
Orbit Nasopharynx Middle ear/mastoid Sinonasal cavity
34
which type of rhabdo has better prognosis: embryonal or alveolar?
embryonal (75% of them)
35
what is Von-Hippel-Lindau
° Autosomal dominant ° Hemangioblastomas of CNS and retinas, renal cysts/carcinoma, pheochromocytoma, pancreatic cysts, papillary cystadenomas of epididymis ° Associated with endolymphatic sac tumors
36
What is maffucci syndrome?
benign cartilagenous overgrowths
37
What are the two most common syndromes associated with PRS?
Stickler, velocardiofacial syndromes