Infections N Bone Disorders Flashcards

1
Q

Heerfordt syndrome

A

Uveoparotid fever

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2
Q

Behcets syndrome

A

Recurrent oral ulcers
Recurrent genital ulcers
Ocular inflammation

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3
Q

Reiters syndrome

A

muac
Multiple oral ulcers
Urethritis
Arthritis
Conjunctivitis

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4
Q

Ramsay Hunt syndrome

A

Herpes zoster infection of geniculate ganglion involving ext ear and oral mucosa (facial paralysis n facial blisters)

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5
Q

Crouzon syndrome / cranio facial dysostosis

A

Prognathic mandible, hypoplastic maxilla, high arched palate or parrot beak appearance
Hypertelorism

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6
Q

Apert syndrome

A

Syndactaly involving hands and feet (mitten hands & sock feet) + features similar to Crouzon syndrome

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7
Q

Treacher Collin syndrome

A

Mandibulofacial dysostosis / Franschetti syndrome

Hypoplasia of mandible and malar bone, macrostomia,
(OR) malformation of
external ear, high arched palate, bird or fish like face and antimongoloid
slant with coloboma of lower eyelids.

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8
Q

Pierre Robin Syndrome

A

Cleft palate
Micrognathia
Glossoptosis

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9
Q

Marfan Syndrome

A

Long thin extremities,
hyper extensibility of joints,
spidery fingers.
arachnodactyly,
bifid uvula and CVS complications.

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10
Q

Down Syndrome

A

Trisomy 21/ ongolism

Hypermobility, macroglossia, flat face, large anterior fontanelle, sexual
underdevelopment and cardiac abnormalities.

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11
Q

Van Buchem Syndrome

A

Generalised cortical hyperostosis.

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12
Q

Gorham Syndrome

A

Massive osteolysis or vanishing bone.

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13
Q

Albright Syndrome

A

Precocious puberty
Polyostotic fibrous dysplasia
Café-au-lait pigmentation.

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14
Q

Caffey-Silverman Syndrome

A

Infantile hyperostosis, dysphagia, hyperirritability, increased alkaline
phosphatase.

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15
Q

Costen Syndrome

A

Tinnitus, otalgia, headache, dizziness, burning tongue and throat.

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16
Q

Myofacial Pain Dysfunction Syndrome

A

Masticatory muscle tenderness & pain
limitation of motion
clicking or propping noise.

17
Q

PFAPA syndrome

A

Periodic fever
Aphthous stomatitis
Pharyngitis
Adenitis

18
Q

Rotar syndrome
Vs
Dubin Johnson syndrome

A

autosomal recessive disease and a rare cause of mixed direct (conjugated) and indirect (unconjugated) hyperbilirubinemia
—————————
Intermittent jaundice caused by defect in gene ABCC2 protein , doesnt transport