Down syndrome differential diagnosis: Difference between revisions
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{| class="wikitable" | {| class="wikitable" | ||
! rowspan="2" |Fetal chromosomal abnormality | ! rowspan="2" align="center" style="background:#4479BA; color: #FFFFFF;" + |Fetal chromosomal abnormality | ||
! colspan="4" |Quad screen results | ! colspan="4" align="center" style="background:#4479BA; color: #FFFFFF;" + |Quad screen results | ||
! rowspan="2" |'''Pregnancy associated protein-A (PAPP-A)''' | ! rowspan="2" align="center" style="background:#4479BA; color: #FFFFFF;" + |'''Pregnancy associated protein-A (PAPP-A)''' | ||
|- | |- | ||
|'''Alfa-fetoprotein (AFP)''' | ! align="center" style="background:#4479BA; color: #FFFFFF;" + |'''Alfa-fetoprotein (AFP)''' | ||
|'''Beta human chorionic gonadotrpin (B-hCG)''' | ! align="center" style="background:#4479BA; color: #FFFFFF;" + |'''Beta human chorionic gonadotrpin (B-hCG)''' | ||
|'''Estriol''' | ! align="center" style="background:#4479BA; color: #FFFFFF;" + |'''Estriol''' | ||
|'''Inhibin A''' | ! align="center" style="background:#4479BA; color: #FFFFFF;" + |'''Inhibin A''' | ||
|- | |- | ||
|Down syndrome (trisomy 21) | |Down syndrome (trisomy 21) | ||
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{| class="wikitable" | {| class="wikitable" | ||
! rowspan="2" |Congenital condition | ! rowspan="2" align="center" style="background:#4479BA; color: #FFFFFF;" + |Congenital condition | ||
! colspan="14" |Physical examination | ! colspan="14" align="center" style="background:#4479BA; color: #FFFFFF;" + |Physical examination | ||
|- | |- | ||
|'''Hypotonia''' | ! align="center" style="background:#4479BA; color: #FFFFFF;" + |'''Hypotonia''' | ||
|'''Poor feeding''' | ! align="center" style="background:#4479BA; color: #FFFFFF;" + |'''Poor feeding''' | ||
|'''Poor growth''' | ! align="center" style="background:#4479BA; color: #FFFFFF;" + |'''Poor growth''' | ||
|'''Dysmorphic features''' | ! align="center" style="background:#4479BA; color: #FFFFFF;" + |'''Dysmorphic features''' | ||
|'''Single palmar crease''' | ! align="center" style="background:#4479BA; color: #FFFFFF;" + |'''Single palmar crease''' | ||
|'''Epicanthal folds''' | ! align="center" style="background:#4479BA; color: #FFFFFF;" + |'''Epicanthal folds''' | ||
|'''Flat occiput and face''' | ! align="center" style="background:#4479BA; color: #FFFFFF;" + |'''Flat occiput and face''' | ||
|'''Seizures''' | ! align="center" style="background:#4479BA; color: #FFFFFF;" + |'''Seizures''' | ||
|'''Dry skin''' | ! align="center" style="background:#4479BA; color: #FFFFFF;" + |'''Dry skin''' | ||
|'''Ophtalmologic examination''' | ! align="center" style="background:#4479BA; color: #FFFFFF;" + |'''Ophtalmologic examination''' | ||
|'''Abundant neck skin''' | ! align="center" style="background:#4479BA; color: #FFFFFF;" + |'''Abundant neck skin''' | ||
|'''Gap between first and second fingers''' | ! align="center" style="background:#4479BA; color: #FFFFFF;" + |'''Gap between first and second fingers''' | ||
|'''Protruding tongue''' | ! align="center" style="background:#4479BA; color: #FFFFFF;" + |'''Protruding tongue''' | ||
|'''Downward turned mouth''' | ! align="center" style="background:#4479BA; color: #FFFFFF;" + |'''Downward turned mouth''' | ||
|- | |- | ||
|Down syndrome | |Down syndrome |
Revision as of 03:59, 21 March 2018
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Differential Diagnosis
Pre-natal differentials
The diagnosis of Down syndrome should be suspected in pre-natal assessment of fetuses on ultrasound examination. Second quad screen showing decreased alfa-fetoprotein (AFP) should raise the suspicion of fetal chromosomal abnormlaity. The following are the differential diagnosis of decreased AFP levels during a first trimester quad screen:
Fetal chromosomal abnormality | Quad screen results | Pregnancy associated protein-A (PAPP-A) | |||
---|---|---|---|---|---|
Alfa-fetoprotein (AFP) | Beta human chorionic gonadotrpin (B-hCG) | Estriol | Inhibin A | ||
Down syndrome (trisomy 21) | ↓ | ↑ | ↓ | ↑ | ↓ |
Edwards syndrome (trisomy 18) | ↓ | ↓ | ↓ | ↓ or normal | ↓ |
Patau syndrome (trisomy 13) | ↓ | ↓ | ↓ | ↓ | ↓ |
Differentials in newborns and children
In the newborn, Down syndrome should be differentiated from other congenital conditions presenting with hypotonia, poor feeding, poor growth and dysmorphic facial features. The differentials include the following:
Congenital condition | Physical examination | |||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Hypotonia | Poor feeding | Poor growth | Dysmorphic features | Single palmar crease | Epicanthal folds | Flat occiput and face | Seizures | Dry skin | Ophtalmologic examination | Abundant neck skin | Gap between first and second fingers | Protruding tongue | Downward turned mouth | |
Down syndrome | + | + | + | + | + | + | + | + | - |
|
+ | Increased | + | + |
Isolated hypotonia | + | - | - | - | - | - | - | - | - | - | - | - | - | - |
Congenital hypothroidism | + | + | + | + | - | - | - | + | + |
|
- | - | + | - |
Zellwegger syndrome | + | + | + | + | + | + | + | + | - |
|
- | - | - | - |
Down syndrome must be differentiated from other similar conditions which lead to multiple endocrine disorders such as autoimmune polyendocrine syndrome, POEMS syndrome, Hirata syndrome, Kearns–Sayre syndrome and Wolfram syndromes.[1][2][3][4][5]
Disease | Addison's disease | Type 1 diabetes mellitus | Hypothyroidism | Other disorders present |
---|---|---|---|---|
APS type 1 | + | Less common | Less common | Hypoparathyroidism Candidiasis Hypogonadism |
APS type 2 | + | + | + | Hypogonadism Malabsorption |
APS type 3 | - | + | + | Malabsorption |
Thymoma | + | - | + | Myasthenia gravis Cushing syndrome |
Chromosomal abnormalities (Turner syndrome, Down's syndrome) |
- | + | + | Cardiac dysfunction |
Kearns–Sayre syndrome | - | + | - | Myopathy Hypoparathyroidism Hypogonadism |
Wolfram syndrome | - | + | - | Diabetes insipidus Optic atrophy Deafness |
POEMS syndrome | - | + | - | Polyneuropathy Hypogonadism Plasma cell dyscrasias |
References
- ↑ Sherer Y, Bardayan Y, Shoenfeld Y (1997). "Thymoma, thymic hyperplasia, thymectomy and autoimmune diseases (Review)". Int. J. Oncol. 10 (5): 939–43. PMID 21533467.
- ↑ Nozza, Andrea (2017). "POEMS SYNDROME: AN UPDATE". Mediterranean Journal of Hematology and Infectious Diseases. 9 (1): e2017051. doi:10.4084/mjhid.2017.051. ISSN 2035-3006.
- ↑ Maceluch JA, Niedziela M (2006). "The clinical diagnosis and molecular genetics of kearns-sayre syndrome: a complex mitochondrial encephalomyopathy". Pediatr Endocrinol Rev. 4 (2): 117–37. PMID 17342029.
- ↑ Rigoli L, Di Bella C (2012). "Wolfram syndrome 1 and Wolfram syndrome 2". Curr. Opin. Pediatr. 24 (4): 512–7. doi:10.1097/MOP.0b013e328354ccdf. PMID 22790102.
- ↑ Husebye, Eystein S.; Anderson, Mark S. (2010). "Autoimmune Polyendocrine Syndromes: Clues to Type 1 Diabetes Pathogenesis". Immunity. 32 (4): 479–487. doi:10.1016/j.immuni.2010.03.016. ISSN 1074-7613.