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A Syndrome Scrabble
*Corresponding author: Dr. Nitin Choudhary, Department of Anaesthesiology, Pain Medicine and Critical Care, All India Institute of Medical Sciences, New Delhi, India. drnitinchoudhary86@gmail.com
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Received: ,
Accepted: ,
How to cite this article: Kumar M, Magoon R, Choudhary N. A Syndrome Scrabble. J Neonatal Crit Care Anesth. 2024;1:64-6. doi: 10.25259/JNCCA_10_2024
SYNDROME CROSSWORD
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1 The word “Syndrome” derives its origin from this language.
2 Macrosomia, hemihypertrophy, and macroglossia form a triad of this syndrome.
4 Single Palmar Crease seen in Trisomy 21.
5 Congenital His Bundle Tachycardia, otherwise known as _________ Ectopic Tachycardia, which is a rare arrhythmia observed in neonates.
6 >6 of these spots constitute a dermatological sign of Neurofibromatosis type 1.
9 Acronym for this syndrome which also happens to be the other name for neonatal onset multisystem inflammatory disease.
10 A pentalogy formed by the constellation of five congenital midline birth anomalies.
11 A term used to describe long, slender, and spider-like abnormality of the fingers.
15 Trisomy 18 Syndrome.
18 Sequence causing micrognathia, glossoptosis, and cleft palate, resulting in a difficult airway.
20 Classic Triad of cataract, patent ductus arteriosus, and sensorineural deafness, seen in.
22 An autosomal dominant disease linked to arteriohepatic dysplasia.
ACROSS
3 A type of heterotaxy syndrome with findings of right isomerism, like asplenia.
7 Benign idiopathic neonatal seizures are called as _____ day fits.
8 Diagnostic criteria for congenital long QT syndrome.
12 Named facies in William’s Syndrome.
13 A congenital malformation featuring hydrocephalus, posterior fossa cyst, and the absence of the cerebellar vermis.
14 “CHARGE” association is also known as ___________ syndrome.
16 Whistling Face syndrome having features of microstomia.
17 Chromosome 22q11.2 deletion may present with this electrolyte abnormality due to primary hypoparathyroidism.
19 Immotile cilia syndrome.
21 Anemia associated with abnormalities of the gastrointestinal system such as esophageal atresia and tracheoesophageal fistula.
23 Congenital absence or defect of ocular tissue, frequently seen across neonatal syndromes.
24 Syndrome associated with a mutation in neural crest transcription factor TFAP2B, characterized by typical facial and hand anomalies with patent ductus arteriosus.
25 Syndrome deriving its name from the wrinkled appearance of abdominal skin.
SYNDROME CROSSWORD ANSWERS
