Growth hormone deficiency differential diagnosis: Difference between revisions
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|- style="background: #4479BA; color: #FFFFFF; text-align: center;" | |- style="background: #4479BA; color: #FFFFFF; text-align: center;" | ||
! rowspan="2" |Diseases | ! rowspan="2" |Diseases | ||
| rowspan="2" |History and symptoms | |||
| colspan="4" |Physical Examination | | colspan="4" |Physical Examination | ||
! colspan="3" |Laboratory findings | ! colspan="3" |Laboratory findings | ||
|- style="background: #4479BA; color: #FFFFFF; text-align: center;" | |- style="background: #4479BA; color: #FFFFFF; text-align: center;" | ||
!Puberty development | !Puberty development | ||
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|- | |- | ||
| style="background: #DCDCDC; padding: 5px; text-align: center;" |Growth hormone deficiency | | style="background: #DCDCDC; padding: 5px; text-align: center;" |Growth hormone deficiency | ||
| style="background: #F5F5F5; padding: 5px;" | | |||
* adults who are deficient in GH and not replaced compared with those who have normal GH secretion.<sup>[[Growth hormone deficiency history and symptoms#cite note-pmid2245969-4|[4]]]</sup> | |||
* Fractures of the lumbar spine [[Osteopenia|osteopenia.]] | |||
| style="background: #F5F5F5; padding: 5px;" |Delayed | | style="background: #F5F5F5; padding: 5px;" |Delayed | ||
| style="background: #F5F5F5; padding: 5px;" |Decreased | | style="background: #F5F5F5; padding: 5px;" |Decreased | ||
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* GH1 gene mutations | * GH1 gene mutations | ||
| style="background: #F5F5F5; padding: 5px;" |Low | | style="background: #F5F5F5; padding: 5px;" |Low | ||
|- | |- | ||
| style="background: #DCDCDC; padding: 5px; text-align: center;" |[[Achondroplasia]] | | style="background: #DCDCDC; padding: 5px; text-align: center;" |[[Achondroplasia]] | ||
| style="background: #F5F5F5; padding: 5px;" |Short arms and legs | |||
| style="background: #F5F5F5; padding: 5px;" |Normal | | style="background: #F5F5F5; padding: 5px;" |Normal | ||
| style="background: #F5F5F5; padding: 5px;" |Decreased | | style="background: #F5F5F5; padding: 5px;" |Decreased | ||
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FGFR3 gene mutations | FGFR3 gene mutations | ||
| style="background: #F5F5F5; padding: 5px;" |Normal | | style="background: #F5F5F5; padding: 5px;" |Normal | ||
|- | |- | ||
| style="background: #DCDCDC; padding: 5px; text-align: center;" |Familial short stature | | style="background: #DCDCDC; padding: 5px; text-align: center;" |Familial short stature | ||
| style="background: #F5F5F5; padding: 5px;" | | | style="background: #F5F5F5; padding: 5px;" | | ||
| style="background: #F5F5F5; padding: 5px;" |Normal | |||
| style="background: #F5F5F5; padding: 5px;" |Decreased | | style="background: #F5F5F5; padding: 5px;" |Decreased | ||
| style="background: #F5F5F5; padding: 5px;" |Decreased | | style="background: #F5F5F5; padding: 5px;" |Decreased | ||
| style="background: #F5F5F5; padding: 5px;" |Normal | | style="background: #F5F5F5; padding: 5px;" |Normal | ||
| style="background: #F5F5F5; padding: 5px;" |Normal | | style="background: #F5F5F5; padding: 5px;" |Normal | ||
| style="background: #F5F5F5; padding: 5px;" |Normal | | style="background: #F5F5F5; padding: 5px;" |Normal | ||
| style="background: #F5F5F5; padding: 5px;" | | | style="background: #F5F5F5; padding: 5px;" |Normal | ||
|- | |- | ||
|Constitutional growth delay | |Constitutional growth delay | ||
|Family history of delayed growth and puberty | |||
|Delayed | |Delayed | ||
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|Normal | |Normal | ||
|Normal | |Normal | ||
|- | |- | ||
| style="background: #DCDCDC; padding: 5px; text-align: center;" |Growth Hormone Resistance | | style="background: #DCDCDC; padding: 5px; text-align: center;" |Growth Hormone Resistance | ||
| style="background: #F5F5F5; padding: 5px;" | | |||
| style="background: #F5F5F5; padding: 5px;" |Delayed | | style="background: #F5F5F5; padding: 5px;" |Delayed | ||
| style="background: #F5F5F5; padding: 5px;" |Decreased | | style="background: #F5F5F5; padding: 5px;" |Decreased | ||
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* IGF-I gene mutations | * IGF-I gene mutations | ||
| style="background: #F5F5F5; padding: 5px;" |Normal | | style="background: #F5F5F5; padding: 5px;" |Normal | ||
|- | |- | ||
|[[Hypothyroidism|Pediatric Hypothyroidism]] | |[[Hypothyroidism|Pediatric Hypothyroidism]] | ||
|Sluggishness, lethargy, cold intolerance, constipation, decreased reflexes | |Sluggishness, lethargy, cold intolerance, constipation, decreased reflexes | ||
|Delayed | |||
|Decreased | |Decreased | ||
|Normal | |Normal | ||
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* Transcription factors NK2 | * Transcription factors NK2 | ||
|Normal | |Normal | ||
|- | |- | ||
| style="background: #DCDCDC; padding: 5px; text-align: center;" |[[Turner syndrome|Turner Syndrome]] | | style="background: #DCDCDC; padding: 5px; text-align: center;" |[[Turner syndrome|Turner Syndrome]] | ||
| style="background: #F5F5F5; padding: 5px;" | | | style="background: #F5F5F5; padding: 5px;" | | ||
* Females only | * Females only | ||
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* Short neck | * Short neck | ||
* Ovarian failure | * Ovarian failure | ||
| style="background: #F5F5F5; padding: 5px;" |Absent | |||
| style="background: #F5F5F5; padding: 5px;" |Decreased | |||
| style="background: #F5F5F5; padding: 5px;" |Decreased | |||
| style="background: #F5F5F5; padding: 5px;" | | |||
| style="background: #F5F5F5; padding: 5px;" |Normal | |||
| style="background: #F5F5F5; padding: 5px;" |45 X0 | |||
| style="background: #F5F5F5; padding: 5px;" |Normal | |||
|- | |- | ||
|[[Silver-Russell Syndrome]] | |[[Silver-Russell Syndrome]] | ||
|hemihypertrophy | |||
|Delayed | |Delayed | ||
|Decreased | |Decreased | ||
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| Unknown defect | | Unknown defect | ||
|Normal | |Normal | ||
|- | |- | ||
|[[Noonan syndrome|Noonan Syndrome]] | |[[Noonan syndrome|Noonan Syndrome]] | ||
|Heart disease | |||
webbed neck | |||
cryptorchidism | |||
intellectual disability, | |||
|Delayed | |Delayed | ||
|Decreased | |Decreased | ||
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|PTPN11 and SOS1 genes abnormality | |PTPN11 and SOS1 genes abnormality | ||
|Normal | |Normal | ||
|- | |- | ||
|Short stature from [[Child Abuse|abuse]] and neglect | |Short stature from [[Child Abuse|abuse]] and neglect | ||
| | |||
| | | | ||
| | | | ||
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|Normal | |Normal | ||
|No | |No | ||
| | | | ||
|- | |- | ||
|Short stature accompanying systemic disease | |Short stature accompanying systemic disease | ||
| | |||
|Delayed | |Delayed | ||
|Decreased | |Decreased | ||
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|Normal | |Normal | ||
|Normal | |Normal | ||
|} | |} | ||
Revision as of 18:23, 17 August 2017
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Differentiating Growth hormone deficiency from other Diseases |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Mohammed Abdelwahed M.D[2]
Overview
Differentiating Growth Hormone Deficiency from other Diseases
Growth hormone deficiency in children must be differentiated from other diseases that cause short stature in children such as:
- Achondroplasia
- Constitutional Growth Delay
- Familial short stature
- Growth Hormone Resistance
- Noonan Syndrome
- Panhypopituitarism
- Pediatric Hypothyroidism
- Short stature accompanying systemic disease
- Short stature from abuse and neglect
- Silver-Russell Syndrome
- Turner Syndrome
Diseases | History and symptoms | Physical Examination | Laboratory findings | |||||
---|---|---|---|---|---|---|---|---|
Puberty development | Height velocity | Parents height | Characteristic facies | Bone age | Genetic analysis | GH level | ||
Growth hormone deficiency |
|
Delayed | Decreased | Normal |
|
Dlayed |
|
Low |
Achondroplasia | Short arms and legs | Normal | Decreased | Decreased | midface hypoplasia | Delayed |
FGFR3 gene mutations |
Normal |
Familial short stature | Normal | Decreased | Decreased | Normal | Normal | Normal | Normal | |
Constitutional growth delay | Family history of delayed growth and puberty | Delayed
. |
Normal | Normal | Normal | Normal | Normal | Normal |
Growth Hormone Resistance | Delayed | Decreased |
|
Delayed |
|
Normal | ||
Pediatric Hypothyroidism | Sluggishness, lethargy, cold intolerance, constipation, decreased reflexes | Delayed | Decreased | Normal |
|
Delayed |
Mutations in:
|
Normal |
Turner Syndrome |
|
Absent | Decreased | Decreased | Normal | 45 X0 | Normal | |
Silver-Russell Syndrome | hemihypertrophy | Delayed | Decreased | Decreased | Prominent forehead, triangular face, downturned corners of the mouth | Normal | Unknown defect | Normal |
Noonan Syndrome | Heart disease
webbed neck cryptorchidism intellectual disability, |
Delayed | Decreased | Decreased | Minor facial dysmorphism | Normal | PTPN11 and SOS1 genes abnormality | Normal |
Short stature from abuse and neglect |
|
Normal | No | |||||
Short stature accompanying systemic disease | Delayed | Decreased | Normal | Delayed | Normal | Normal |