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  
! rowspan="2" |History and Symptoms
|- 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: #F5F5F5; padding: 5px;" |
|-
|-
| 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: #F5F5F5; padding: 5px;" |Short arms and legs
|-
|-
| 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;" |Short parents
| style="background: #F5F5F5; padding: 5px;" |
 
| style="background: #F5F5F5; padding: 5px;" |Normal
Adult height short for population
| 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;" |
| 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
|Family history of delayed growth and puberty
|-
|-
| 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
| style="background: #F5F5F5; padding: 5px;" |
|-
|-
|[[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;" |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
| 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
|hemihypertrophy
|-
|-
|[[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
|Heart disease
webbed neck
cryptorchidism
intellectual disability,
|-
|-
|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

Growth hormone deficiency Microchapters

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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:

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
  • adults who are deficient in GH and not replaced compared with those who have normal GH secretion.[4]
  • Fractures of the lumbar spine osteopenia.
Delayed Decreased Normal
  • Doll-like fat distribution pattern
  • Immature face with under developed nasal bridge
  • Infantile voice
Dlayed
  • POU1F1 gene mutations 
  • GH1 gene mutations
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
  • Face small in relation to head circumference
  • Delayed dentition
Delayed
  • Growth hormone receptor mutations
  • IGF-I gene mutations
Normal
Pediatric Hypothyroidism Sluggishness, lethargy, cold intolerance, constipation, decreased reflexes Delayed Decreased Normal
  • Puffy facies
  • Macroglossia
  • Large fontanels
  • Micrognathia
Delayed

Mutations in:

  • Paired box 8 (PAX8)
  • thyroid Transcription factor-2 (TTF2
  • Transcription factors NK2
Normal
Turner Syndrome
  • Females only
  • Infertility
  • Webbed neck
  • Widely spaced nipples
  • broad chest
  • Genu valgum
  • Short neck
  • Ovarian failure  
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
  • Failure to thrive
  • Poor dentition
  • Bad hyegine
  • Sad Affect
Normal No
Short stature accompanying systemic disease Delayed Decreased Normal Delayed Normal Normal

References

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